Award-winning facility looking for a full time, permanent medical technologist! Quick Facts Night and evening shift Medical Technologist (MT) ASCP certification preferred New York State license required BS degree required Prefer 6+ years of experience Generalist position $4500 retention bonus Great compensation Full benefits Short drive away from Syracuse and Ithica SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. SPECIAL NOTES: Must have a New York State License as a Medical Technologist. (No exceptions) Come join this advanced, award-winning hospital! One evening shift and one night shift available for a generalist position. A bachelor's degree in medical technology is required. Must hold a current New York State medical technologist license. ASCP certification is preferred. They are offering a great salary and full benefits. They prefer at least 6 years of lab experience. Enjoy living an unhurried simple life in this rural, affordable area with a friendly atmosphere. Capture the beauty of all of the seasons with a variety of activities for everyone to enjoy year round. Several parks and attractions in town to enjoy. Only a short drive away from both Syracuse and Ithica. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Nov 05, 2017
Full time
Award-winning facility looking for a full time, permanent medical technologist! Quick Facts Night and evening shift Medical Technologist (MT) ASCP certification preferred New York State license required BS degree required Prefer 6+ years of experience Generalist position $4500 retention bonus Great compensation Full benefits Short drive away from Syracuse and Ithica SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. SPECIAL NOTES: Must have a New York State License as a Medical Technologist. (No exceptions) Come join this advanced, award-winning hospital! One evening shift and one night shift available for a generalist position. A bachelor's degree in medical technology is required. Must hold a current New York State medical technologist license. ASCP certification is preferred. They are offering a great salary and full benefits. They prefer at least 6 years of lab experience. Enjoy living an unhurried simple life in this rural, affordable area with a friendly atmosphere. Capture the beauty of all of the seasons with a variety of activities for everyone to enjoy year round. Several parks and attractions in town to enjoy. Only a short drive away from both Syracuse and Ithica. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Exciting opportunity for a full time, permanent medical technologist or medical laboratory technician! Quick Facts Evening or night shift MT/MLT BS degree in Medical Technology or equivalent/AS degree in MLT or equivalent ASCP certified or eligible Generalist position New grads welcome to apply Negotiable relocation bonus Average sign-on bonus of $1000-$3000, possibly more Excellent compensation Great outdoor activities SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist or a Medical Laboratory Technician. Generalist position at a small critical access hospital. Multiple evening shifts and one night shift available. Bachelor's degree in medical technology or equivalent required for MT position. Associate's degree in medical laboratory technology or equivalent required. Must also be ASCP certified or eligible. They are offering a very competitive salary and new grads are welcome to apply. They recently completed a $40 Million addition/renovation to the facility. Located in the gorgeous hilly plains of western Nebraska. Home of the #2 wackiest attraction in the US, carhenge (a replica of Stonehenge). Numerous parks, museums, and outdoor activities to partake in! A short commute from Nebraska National Forest and Oglala National Grassland. If you love the outdoors and nature, you'll love it here. Small town with a booming downtown area that takes great pride in its history - many of the brick buildings from the 1900's are still standing strong. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Nov 05, 2017
Full time
Exciting opportunity for a full time, permanent medical technologist or medical laboratory technician! Quick Facts Evening or night shift MT/MLT BS degree in Medical Technology or equivalent/AS degree in MLT or equivalent ASCP certified or eligible Generalist position New grads welcome to apply Negotiable relocation bonus Average sign-on bonus of $1000-$3000, possibly more Excellent compensation Great outdoor activities SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist or a Medical Laboratory Technician. Generalist position at a small critical access hospital. Multiple evening shifts and one night shift available. Bachelor's degree in medical technology or equivalent required for MT position. Associate's degree in medical laboratory technology or equivalent required. Must also be ASCP certified or eligible. They are offering a very competitive salary and new grads are welcome to apply. They recently completed a $40 Million addition/renovation to the facility. Located in the gorgeous hilly plains of western Nebraska. Home of the #2 wackiest attraction in the US, carhenge (a replica of Stonehenge). Numerous parks, museums, and outdoor activities to partake in! A short commute from Nebraska National Forest and Oglala National Grassland. If you love the outdoors and nature, you'll love it here. Small town with a booming downtown area that takes great pride in its history - many of the brick buildings from the 1900's are still standing strong. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Exciting opportunity for a full time, permanent medical technologist! QUICK FACTS Evening shift generalist MT ASCP certification or equivalent required BS degree in Medical Technology preferred At least one year of experience required Competitive pay Full benefits Sign-on bonus and relocation assistance offered Beautiful mountain scenery Low cost of living SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. Award-winning non-profit hospital in the beautiful mountains of Arizona is looking for a generalist medical technologist for the evening shift. ASCP certification is preferred but would also accept an equivalent certification. BS degree in Medical technology is required. At least one year of experience is required. They are offering full benefits, competitive pay, sign-on bonus and relocation assistance. Show Low is The Gateway to Arizona's White Mountains and the quality of life here is unequaled anywhere. The area is famous for its world class hunting and fishing opportunities. There are over 2 million acres of National Forest land adjacent to Show Low and over 40 lakes and streams in the immediate area. Camping and hiking are popular activities as well as numerous other outdoor activities. Show Low also offers a wealth of dining and shopping opportunities from the national chains to more regional fare. It is truly a city that blends the charm of a small town with all the comforts of a larger city. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Nov 05, 2017
Full time
Exciting opportunity for a full time, permanent medical technologist! QUICK FACTS Evening shift generalist MT ASCP certification or equivalent required BS degree in Medical Technology preferred At least one year of experience required Competitive pay Full benefits Sign-on bonus and relocation assistance offered Beautiful mountain scenery Low cost of living SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. Award-winning non-profit hospital in the beautiful mountains of Arizona is looking for a generalist medical technologist for the evening shift. ASCP certification is preferred but would also accept an equivalent certification. BS degree in Medical technology is required. At least one year of experience is required. They are offering full benefits, competitive pay, sign-on bonus and relocation assistance. Show Low is The Gateway to Arizona's White Mountains and the quality of life here is unequaled anywhere. The area is famous for its world class hunting and fishing opportunities. There are over 2 million acres of National Forest land adjacent to Show Low and over 40 lakes and streams in the immediate area. Camping and hiking are popular activities as well as numerous other outdoor activities. Show Low also offers a wealth of dining and shopping opportunities from the national chains to more regional fare. It is truly a city that blends the charm of a small town with all the comforts of a larger city. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
GARANT Türen und Zargen GmbH
Ichtershausen, Germany
Ihr Ansprechpartnerin: Lisa Deckert GARANT Türen und Zargen GmbH OT Ichtershausen Garantstraße 1, Gewerbepark Thörey 99334 Amt Wachsenburg T 036202/91-0 E Leiter Entwicklung/ Konstruktion (m/w) Ihre Aufgaben • Fachliche und disziplinarische Führung der Mitarbeiter der Abteilung Entwicklung/ Konstruktion • Begleitung und Überwachung des Entwicklungsprozesses von technischen Türen von der Planung bis zur Serienreife • Anwendung von Methoden zur Produktoptimierung • Leitung und Überwachung der Entwicklungsprojekte • Enge Zusammenarbeit mit den internen Fachabteilungen und anderen Entwicklungsbereichen im Konzern • Technische Unterstützung des Vertriebs Ihr Profil • Abgeschlossenes technisches Studium, idealerweise im Bereich Holztechnik • mehrjährige Berufserfahrung in der fertigenden Industrie, idealerweise im Bereich der Holzverarbeitung • Kommunikationsstarke und erfahrene Führungspersönlichkeit • Erfahrungen im Projektmanagement • Hohes technisches Verständnis und unternehmerisches Denken • Gute Kenntnisse im Umgang mit CAD-Software (AutoCAD), sowie ERP-System und MS-Office • Selbstständiger, strukturierter, lösungsorientierter und eigenverantwortlicher Arbeitsstil • Teamfähigkeit Das können Sie von uns erwarten: • Interessante und eigenverantwortliche Tätigkeit mit guten Entwicklungschancen • Motiviertes Team, Flexible Arbeitszeiten, Pausenversorgung durch die Kantine und diverse Sozialleistungen • Angemessene Vergütung gemäß Haustarifvertrag, orientiert am Flächentarifvertrag der IG Metall Thüringen Haben wir Ihr Interesse geweckt? Dann freuen wir uns auf Ihre aussagekräftigen Bewerbungsunterlagen. Bitte senden Sie uns Ihre vollständigen Bewerbungsunterlagen, vorzugsweise per E-Mail, unter Angabe Ihrer Lohnvorstellung und Ihres frühestmöglichen Eintrittstermins an: Die GARANT Türen und Zargen GmbH mit Standort im Gewerbegebiet Erfurter Kreuz zählt als international etablierter Hersteller von hochwertigen Innentüren zu den führenden Türenherstellern Europas. GARANT ist eine Gesellschaft der Arbonia AG, einem fokussiertem Gebäudezulieferer mit insgesamt rund 8500 Mitarbeitern. Wir beschäftigen ca. 480 Mitarbeiter in Ichtershausen und würden uns freuen, wenn Sie demnächst dazu gehören. Wir suchen Sie als Führungskraft für unsere Abteilung Entwicklung/Konstruktion als
Nov 05, 2017
Full time
Ihr Ansprechpartnerin: Lisa Deckert GARANT Türen und Zargen GmbH OT Ichtershausen Garantstraße 1, Gewerbepark Thörey 99334 Amt Wachsenburg T 036202/91-0 E Leiter Entwicklung/ Konstruktion (m/w) Ihre Aufgaben • Fachliche und disziplinarische Führung der Mitarbeiter der Abteilung Entwicklung/ Konstruktion • Begleitung und Überwachung des Entwicklungsprozesses von technischen Türen von der Planung bis zur Serienreife • Anwendung von Methoden zur Produktoptimierung • Leitung und Überwachung der Entwicklungsprojekte • Enge Zusammenarbeit mit den internen Fachabteilungen und anderen Entwicklungsbereichen im Konzern • Technische Unterstützung des Vertriebs Ihr Profil • Abgeschlossenes technisches Studium, idealerweise im Bereich Holztechnik • mehrjährige Berufserfahrung in der fertigenden Industrie, idealerweise im Bereich der Holzverarbeitung • Kommunikationsstarke und erfahrene Führungspersönlichkeit • Erfahrungen im Projektmanagement • Hohes technisches Verständnis und unternehmerisches Denken • Gute Kenntnisse im Umgang mit CAD-Software (AutoCAD), sowie ERP-System und MS-Office • Selbstständiger, strukturierter, lösungsorientierter und eigenverantwortlicher Arbeitsstil • Teamfähigkeit Das können Sie von uns erwarten: • Interessante und eigenverantwortliche Tätigkeit mit guten Entwicklungschancen • Motiviertes Team, Flexible Arbeitszeiten, Pausenversorgung durch die Kantine und diverse Sozialleistungen • Angemessene Vergütung gemäß Haustarifvertrag, orientiert am Flächentarifvertrag der IG Metall Thüringen Haben wir Ihr Interesse geweckt? Dann freuen wir uns auf Ihre aussagekräftigen Bewerbungsunterlagen. Bitte senden Sie uns Ihre vollständigen Bewerbungsunterlagen, vorzugsweise per E-Mail, unter Angabe Ihrer Lohnvorstellung und Ihres frühestmöglichen Eintrittstermins an: Die GARANT Türen und Zargen GmbH mit Standort im Gewerbegebiet Erfurter Kreuz zählt als international etablierter Hersteller von hochwertigen Innentüren zu den führenden Türenherstellern Europas. GARANT ist eine Gesellschaft der Arbonia AG, einem fokussiertem Gebäudezulieferer mit insgesamt rund 8500 Mitarbeitern. Wir beschäftigen ca. 480 Mitarbeiter in Ichtershausen und würden uns freuen, wenn Sie demnächst dazu gehören. Wir suchen Sie als Führungskraft für unsere Abteilung Entwicklung/Konstruktion als
Washington Hospital Center
1331 Pennsylvania Ave NW, Washington, DC 20004, USA
GENERAL SUMMARY Is the staff member of the John J. Lynch Center for Ethics sharing primary responsibility for the John J. Lynch Center for Ethic's Clinical Ethics Consultation Service. Serves as Administrator of the subcommittees, specifically at a minimum, the consultation, and education subcommittees. Provides support and ethical guidance to various subcommittees within the Medstar Washington Hospital Center (MWHC), Medstar Health, and to other organizations locally and nationally. Coordinates closely with all other members of the John J Lynch Center for Ethics on all Center functions. May speak as a MWHC ethics public representative and may serve on various community and national boards after coordinating with the Center Director about such appointments or volunteer positions. Reports to the Director of John J Lynch Center for Ethics. MINIMUM REQUIREMENTS EDUCATION: Master's degree in Philosophy, Ethics, Bioethics, Theology, or an equivalent discipline is required. Doctorate degree in Philosophy, Ethics, Bioethics, Theology or an equivalent terminal degree (ie JD, MD) is preferred. Successful completion of a fellowship in clinical ethics is highly preferred. PRIOR EXPERIENCE: Approximately two to three years of progressively more responsible job related experience. Previous clinical ethics consultation experience highly preferred. CERTIFICATION/REGISTRATION/LICENSURE: No special certification, registration, or licensure is required. Associated topics: customer service, event organizer, liaison, liasion, minister, pastor, priest, supportive service, teacher, vocational support/training
Nov 05, 2017
Full time
GENERAL SUMMARY Is the staff member of the John J. Lynch Center for Ethics sharing primary responsibility for the John J. Lynch Center for Ethic's Clinical Ethics Consultation Service. Serves as Administrator of the subcommittees, specifically at a minimum, the consultation, and education subcommittees. Provides support and ethical guidance to various subcommittees within the Medstar Washington Hospital Center (MWHC), Medstar Health, and to other organizations locally and nationally. Coordinates closely with all other members of the John J Lynch Center for Ethics on all Center functions. May speak as a MWHC ethics public representative and may serve on various community and national boards after coordinating with the Center Director about such appointments or volunteer positions. Reports to the Director of John J Lynch Center for Ethics. MINIMUM REQUIREMENTS EDUCATION: Master's degree in Philosophy, Ethics, Bioethics, Theology, or an equivalent discipline is required. Doctorate degree in Philosophy, Ethics, Bioethics, Theology or an equivalent terminal degree (ie JD, MD) is preferred. Successful completion of a fellowship in clinical ethics is highly preferred. PRIOR EXPERIENCE: Approximately two to three years of progressively more responsible job related experience. Previous clinical ethics consultation experience highly preferred. CERTIFICATION/REGISTRATION/LICENSURE: No special certification, registration, or licensure is required. Associated topics: customer service, event organizer, liaison, liasion, minister, pastor, priest, supportive service, teacher, vocational support/training
Quality Manager Lindsay Corporation manufactures and markets water management equipment and services including irrigation systems, pump stations, filtration, and M2M controls designed to increase or stabilize crop production while conserving water, energy, and labor, and that also provide efficiency benefits in various industrial applications. Our Transportation Solutions business manufactures and markets infrastructure and road safety products, designed to make roadways and railways safer during expansion and renovation. Through our portfolio of products and services, we strive to meet the needs of a growing world population. When you join our team, you can expect to make a difference in the work you do every day. We have an exciting opportunity for a Quality Manager that will ensure all quality systems are intact at largest manufacturing plant in Lindsay, NE. This integral role will oversee a team of individuals that will various customer's requests, resolutions, certifications, and warranty information. The role will handle quality metrics, costs savings, machine calibration, and environmental management. We are looking for an individual that demonstrates a fire in the belly that is interested in making an immediate impact and building out a team from good to great. This role will interact with senior leadership and have opportunities for growth! Accountabilities include: Develop fact-based analysis for decision making. Make proactive decisions in a timely manner Demonstrate customer vision and advocacy. Be willing to take ownership and resolve the issues Demonstrate courage in identifying and addressing issues. Asks for help or assistance when needed Maintain the Quality Management System in compliance with ISO 9001 requirements Manage company needs for Inspection, Gage Calibrations, ISO Training and Document Control requirements Expectations: Demonstrate a passion for process integrity with a commitment to quality, strive to exceed expectations, always work with safety in mind, ready to make an immediate impact and professionally represent the company Develop fact-based analysis for decision making Make decisions in a timely manner, being proactive Be willing to take ownership and resolve their issues Demonstrate initiative and a strong sense of urgency in the daily conduct of business Requirements: Bachelor's Degree in Engineering with minimum 10 years quality management experience Management of the quality function in an ISO 9001 manufacturing facility is required Thorough understanding of engineering drawings and specifications Thorough knowledge of Quality Systems such as SPC, Lean/Six Sigma, CIP and the ability to inspect and determine acceptability of electrical and mechanical components Thorough understanding of manufacturing processes and capabilities in a metal fabrication environment Successful day-to-day management of ISO systems, audits, and certification. Strong leadership skills, comfortable training Internal Audit Teams and holding Management Reviews with the Leadership Team Ability to assess team and individual performance and determine & implement developmental needs Demonstrated ability to drive change and implement quality program improvements Demonstrated success in managing a supplier certification process Experience managing the warranty process with track record of identifying and driving corrective actions Why join Lindsay? Lindsay offers a comprehensive benefits package. Eligible employees are offered standard company benefits package including company paid vacation, tuition reimbursement, paid holidays and life insurance; in addition, 401(k) with match, medical, dental, vision, disability insurance, flex spending accounts, and a stock purchase plan. We encourage a healthy lifestyle with fitness club membership benefits, wellness programs and non-tobacco user incentives. Lindsay Corporation is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, veteran status or any other protected factor under federal, state or local law. Category: Quality Control , Keywords: Quality Control / Quality Assurance Manager
Nov 05, 2017
Full time
Quality Manager Lindsay Corporation manufactures and markets water management equipment and services including irrigation systems, pump stations, filtration, and M2M controls designed to increase or stabilize crop production while conserving water, energy, and labor, and that also provide efficiency benefits in various industrial applications. Our Transportation Solutions business manufactures and markets infrastructure and road safety products, designed to make roadways and railways safer during expansion and renovation. Through our portfolio of products and services, we strive to meet the needs of a growing world population. When you join our team, you can expect to make a difference in the work you do every day. We have an exciting opportunity for a Quality Manager that will ensure all quality systems are intact at largest manufacturing plant in Lindsay, NE. This integral role will oversee a team of individuals that will various customer's requests, resolutions, certifications, and warranty information. The role will handle quality metrics, costs savings, machine calibration, and environmental management. We are looking for an individual that demonstrates a fire in the belly that is interested in making an immediate impact and building out a team from good to great. This role will interact with senior leadership and have opportunities for growth! Accountabilities include: Develop fact-based analysis for decision making. Make proactive decisions in a timely manner Demonstrate customer vision and advocacy. Be willing to take ownership and resolve the issues Demonstrate courage in identifying and addressing issues. Asks for help or assistance when needed Maintain the Quality Management System in compliance with ISO 9001 requirements Manage company needs for Inspection, Gage Calibrations, ISO Training and Document Control requirements Expectations: Demonstrate a passion for process integrity with a commitment to quality, strive to exceed expectations, always work with safety in mind, ready to make an immediate impact and professionally represent the company Develop fact-based analysis for decision making Make decisions in a timely manner, being proactive Be willing to take ownership and resolve their issues Demonstrate initiative and a strong sense of urgency in the daily conduct of business Requirements: Bachelor's Degree in Engineering with minimum 10 years quality management experience Management of the quality function in an ISO 9001 manufacturing facility is required Thorough understanding of engineering drawings and specifications Thorough knowledge of Quality Systems such as SPC, Lean/Six Sigma, CIP and the ability to inspect and determine acceptability of electrical and mechanical components Thorough understanding of manufacturing processes and capabilities in a metal fabrication environment Successful day-to-day management of ISO systems, audits, and certification. Strong leadership skills, comfortable training Internal Audit Teams and holding Management Reviews with the Leadership Team Ability to assess team and individual performance and determine & implement developmental needs Demonstrated ability to drive change and implement quality program improvements Demonstrated success in managing a supplier certification process Experience managing the warranty process with track record of identifying and driving corrective actions Why join Lindsay? Lindsay offers a comprehensive benefits package. Eligible employees are offered standard company benefits package including company paid vacation, tuition reimbursement, paid holidays and life insurance; in addition, 401(k) with match, medical, dental, vision, disability insurance, flex spending accounts, and a stock purchase plan. We encourage a healthy lifestyle with fitness club membership benefits, wellness programs and non-tobacco user incentives. Lindsay Corporation is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, veteran status or any other protected factor under federal, state or local law. Category: Quality Control , Keywords: Quality Control / Quality Assurance Manager
Full time, permanent director of lab opportunity located on the gorgeous west coast of Florida Quick Facts Day shift director of lab Current FL state supervisor license required Master's degree in a related area required 10+ years of lab experience required Previous director level experience required Gorgeous location Competitive compensation Excellent benefits Less than 2 hours from both Tampa and Orlando SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist or a Medical Laboratory Technician. SPECIAL NOTES: Must have a Florida State Supervisor License. (No exceptions) Day shift lab director position at an award winning hospital. Must have a Florida State supervisor license. The facility requires a candidate to have a master's degree in a related area, at least 10 years of lab experience, and have previous director level experience. They are offering competitive pay, comprehensive benefits, and relocation assistance. Located on the gulf coast of Florida, less than 2 hours north of Tampa. Also within 2 hours of Orlando. Absolutely breathtaking location on the water. If you like the water, this town has plenty of it! Numerous rivers, springs, as well as the bay to partake in swimming, fishing, and other water sports. If you've ever wanted to swim with manatees, this is your chance! The town has excellent schools, convenient shopping, acclaimed antiquing, a golf course, good restaurants featuring local seafood and produce, a Heritage Village with interesting shops, and more. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Nov 04, 2017
Full time
Full time, permanent director of lab opportunity located on the gorgeous west coast of Florida Quick Facts Day shift director of lab Current FL state supervisor license required Master's degree in a related area required 10+ years of lab experience required Previous director level experience required Gorgeous location Competitive compensation Excellent benefits Less than 2 hours from both Tampa and Orlando SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist or a Medical Laboratory Technician. SPECIAL NOTES: Must have a Florida State Supervisor License. (No exceptions) Day shift lab director position at an award winning hospital. Must have a Florida State supervisor license. The facility requires a candidate to have a master's degree in a related area, at least 10 years of lab experience, and have previous director level experience. They are offering competitive pay, comprehensive benefits, and relocation assistance. Located on the gulf coast of Florida, less than 2 hours north of Tampa. Also within 2 hours of Orlando. Absolutely breathtaking location on the water. If you like the water, this town has plenty of it! Numerous rivers, springs, as well as the bay to partake in swimming, fishing, and other water sports. If you've ever wanted to swim with manatees, this is your chance! The town has excellent schools, convenient shopping, acclaimed antiquing, a golf course, good restaurants featuring local seafood and produce, a Heritage Village with interesting shops, and more. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Fantastic opportunity for a full time, permanent blood bank medical technologist! QUICK FACTS Evening shift blood bank MT BS degree in Medical Technology or equivalent ASCP certification or equivalent required Prior blood banking experience required Competitive Pay and full benefits Less than 5 miles from the beach Located on the Cape Fear River SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. Award-winning regional medical center is in need of an experienced blood bank medical technologist for the evening shift. A BS degree in Medical Technology or equivalent is required. ASCP certification or equivalent is required but candidates who are eligible for ASCP certification will also be considered. Must be certified within 60 days of start date. 1 year training in an accredited medical technology program or 3 years experience in a laboratory under the direction of a board certified pathologist is required. They are offering full benefits and competitive pay. Wilmington is one Southern destination with something for everyone. Explore the city's National Register Historic District, which spans 230-plus blocks of churches, classic architecture, moss-draped live oaks, brick-lined streets and antebellum homes. Enjoy live music, performing arts, and museum exhibitions. Visit Airlie Gardens or stroll along the pedestrian-friendly Riverwalk lined with shops and cafes and the Port City Marina. Then hop aboard a water taxi to the famous World War II Battleship North Carolina or take a scenic cruise or sightseeing tour. Bring your family to ride water slides at Jungle Rapids Family Fun Park or explore further out at one of our three beautiful island beaches. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Nov 04, 2017
Full time
Fantastic opportunity for a full time, permanent blood bank medical technologist! QUICK FACTS Evening shift blood bank MT BS degree in Medical Technology or equivalent ASCP certification or equivalent required Prior blood banking experience required Competitive Pay and full benefits Less than 5 miles from the beach Located on the Cape Fear River SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. Award-winning regional medical center is in need of an experienced blood bank medical technologist for the evening shift. A BS degree in Medical Technology or equivalent is required. ASCP certification or equivalent is required but candidates who are eligible for ASCP certification will also be considered. Must be certified within 60 days of start date. 1 year training in an accredited medical technology program or 3 years experience in a laboratory under the direction of a board certified pathologist is required. They are offering full benefits and competitive pay. Wilmington is one Southern destination with something for everyone. Explore the city's National Register Historic District, which spans 230-plus blocks of churches, classic architecture, moss-draped live oaks, brick-lined streets and antebellum homes. Enjoy live music, performing arts, and museum exhibitions. Visit Airlie Gardens or stroll along the pedestrian-friendly Riverwalk lined with shops and cafes and the Port City Marina. Then hop aboard a water taxi to the famous World War II Battleship North Carolina or take a scenic cruise or sightseeing tour. Bring your family to ride water slides at Jungle Rapids Family Fun Park or explore further out at one of our three beautiful island beaches. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Exciting opportunity for a full time, permanent blood bank medical technologist! QUICK FACTS Day shift blood bank MT BS degree in Medical Technology or equivalent Additional specialty training or course study in blood bank required ASCP certification or equivalent required AABB and/or SBB ASCP preferred 3-5 years of experience full time in blood bank required Competitive pay and full benefits Right next to the coast 1 hour drive from New York City SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist or a Medical Laboratory Technician. Award-winning hospital is searching for a medical technologist blood bank specialist for the day shift with rotating weekend and holiday coverage. At least 3 years of full time experience in blood bank is required. ASCP certification or equivalent is required. AABB and/or SBB ASCP certification is preferred. Additional specialty training or course study in blood bank required. BS degree in medical technology or equivalent is required. They are offering a competitive pay and full benefits. Stamford is located in southwest Connecticut right next to the coast, about an hour drive from New York City. You will find plenty to do in Stamford Downtown. With more than 80 restaurants and clubs, hundreds of stores and services, movie and live theaters, galleries, special events, and more. In Stamford and the surrounding areas, there will never be a shortage of things to do! To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Nov 04, 2017
Full time
Exciting opportunity for a full time, permanent blood bank medical technologist! QUICK FACTS Day shift blood bank MT BS degree in Medical Technology or equivalent Additional specialty training or course study in blood bank required ASCP certification or equivalent required AABB and/or SBB ASCP preferred 3-5 years of experience full time in blood bank required Competitive pay and full benefits Right next to the coast 1 hour drive from New York City SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist or a Medical Laboratory Technician. Award-winning hospital is searching for a medical technologist blood bank specialist for the day shift with rotating weekend and holiday coverage. At least 3 years of full time experience in blood bank is required. ASCP certification or equivalent is required. AABB and/or SBB ASCP certification is preferred. Additional specialty training or course study in blood bank required. BS degree in medical technology or equivalent is required. They are offering a competitive pay and full benefits. Stamford is located in southwest Connecticut right next to the coast, about an hour drive from New York City. You will find plenty to do in Stamford Downtown. With more than 80 restaurants and clubs, hundreds of stores and services, movie and live theaters, galleries, special events, and more. In Stamford and the surrounding areas, there will never be a shortage of things to do! To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Performs accurate and reliable analysis requiring a complex network of steps and variables. Recognizes technical, instrumental or physiological problems, identifies the cause and evaluates alternative solutions where no pre-set criteria are available. Confirms and verifies laboratory results utilizing in-depth knowledge of techniques, principles and instruments. Correlates and interprets data based on knowledge of physiological conditions affecting test results. Establishes and monitors quality assurance programs. Participates in establishing and monitoring performance improvement programs.Minimum RequirementsRequired:MT(ASCP) or equivalent. Will consider a student who is MT(ASCP) eligible.Join the Kansas City region's premiere provider of health services. Equal Opportunity Employer. We hire only non-tobacco users. Associated topics: biomedical, dietician, drug, health, histology, immunology, metabolism, pharmaceutical, pharmacy, toxicologist
Nov 04, 2017
Full time
Performs accurate and reliable analysis requiring a complex network of steps and variables. Recognizes technical, instrumental or physiological problems, identifies the cause and evaluates alternative solutions where no pre-set criteria are available. Confirms and verifies laboratory results utilizing in-depth knowledge of techniques, principles and instruments. Correlates and interprets data based on knowledge of physiological conditions affecting test results. Establishes and monitors quality assurance programs. Participates in establishing and monitoring performance improvement programs.Minimum RequirementsRequired:MT(ASCP) or equivalent. Will consider a student who is MT(ASCP) eligible.Join the Kansas City region's premiere provider of health services. Equal Opportunity Employer. We hire only non-tobacco users. Associated topics: biomedical, dietician, drug, health, histology, immunology, metabolism, pharmaceutical, pharmacy, toxicologist
Want to work at one of the best utilities on the planet? Located in Vancouver Washington, Clark Public Utilities is a nationally ranked electric and water utility with exceptional employees committed to providing outstanding service to our customer-owners. We're recruiting a Business Data Analyst to join our team and help keep us among the very best! You'll use your technology based problem solving skills to help create solutions that streamline our application management processes. You'll use your business experience to help build application workflow processes; design enterprise content management practices; and develop data analytics insights. You'll have 2+ years' experience in supporting a complex technology environment with demonstrated experience in one of several disciplines: automated testing, enterprise content management, data analytics. You'll have a degree, preferably a Bachelor's. You'll demonstrate excellent communication skills, and strong customer service focus. To learn more about the duties and qualifications of this position, go to our website at . Click Careers! Clark Public Utilities offers excellent benefits, an attractive wage, and company incentive programs. Resumes may be submitted to or to Clark Public Utilities, Human Resources, P.O. Box 8900, Vancouver, WA 98668. Equal Opportunity Employer Category: Science , Keywords: Data Analyst
Nov 04, 2017
Full time
Want to work at one of the best utilities on the planet? Located in Vancouver Washington, Clark Public Utilities is a nationally ranked electric and water utility with exceptional employees committed to providing outstanding service to our customer-owners. We're recruiting a Business Data Analyst to join our team and help keep us among the very best! You'll use your technology based problem solving skills to help create solutions that streamline our application management processes. You'll use your business experience to help build application workflow processes; design enterprise content management practices; and develop data analytics insights. You'll have 2+ years' experience in supporting a complex technology environment with demonstrated experience in one of several disciplines: automated testing, enterprise content management, data analytics. You'll have a degree, preferably a Bachelor's. You'll demonstrate excellent communication skills, and strong customer service focus. To learn more about the duties and qualifications of this position, go to our website at . Click Careers! Clark Public Utilities offers excellent benefits, an attractive wage, and company incentive programs. Resumes may be submitted to or to Clark Public Utilities, Human Resources, P.O. Box 8900, Vancouver, WA 98668. Equal Opportunity Employer Category: Science , Keywords: Data Analyst
The Business Analysis and Insights (BAI) Sr. Manager drives business performance and efficiency for Amgen Biosimilars in Oncology. BAI Sr. Manager is a trusted, indispensable advisor to the Executive Director of Brand. He or she is a relentless champion of insights-driven strategy, objective, evidence-based decision making, and effective and efficient commercial activity. The BAI Sr. Manager reports to the Business Analysis & Info (BAI) Business Unit Lead. Job Responsibilities include: * Oversee all US BAI activities, including forecasting, primary market research, competitive intelligence and analytics (national and sub-national) * Develop productive relationships commercial leadership to define BAI objectives, budgets and work plans * Lead a cross functional team of BAI staff (competitive intelligence, payer) to produce proactive, actionable customer and market insights * Ensure commercial leadership understands and accounts for key research results and customer and market insights * Lead the forecasting process for franchise and be able to represent the forecast to commercial leadership * Be a strong "devil's advocate", even with senior commercial staff * Lead initiatives within US BAI to improve existing capabilities and develop new ones * Drives strategic and innovative approaches to key business problems * Ensure that both routine and ad-hoc projects are in compliance with all Amgen SOPs and meet service-level expectations for quality, timeliness, and budget * Manage relationships with external vendors and consultants to enable effective and efficient project execution * Develop productive relationships with cross-functional partners, such as Global BAI, Sales Ops, Global Strategic Sourcing, and Compliance * Conduct primary market research, forecasting & secondary analytics Basic Qualifications: * Doctorate degree and 2 years of analytics experience OR * Master's degree and 4 years of analytics experience OR * Bachelor's degree and 6 years of analytics experience OR * Associate's degree and 10 years of analytics experience OR * High school diploma / GED and 12 years of analytics experience Preferred Qualifications: * Bachelor's degree in marketing, statistics, social, behavioral sciences, or related field of study * 10+ years of experience, including market research, competitive intelligence and/or market analysis * 5+ years of experience managing direct reports * Technical Expertise: Demonstrated ability to translate business questions and needs into actionable research plans and synthesize multiple data sources to answer business questions. * Prior technical forecasting experience or experience managing a forecast * Prior technical experience creating or managing KPI and performance metrics * Innovation: Demonstrated ability to identify and implement new methodologies and data sources to enhance Amgen analytics capabilities * Strong Business Acumen: understands both the markets, brands and broader context (internal and external) of the business. Can translate market research insights and findings into realistic, actionable recommendations * Executive presence: can quickly establish credibility with and influence ED/VP level staff * Strong leadership with a demonstrated ability to build and develop high performing teams, deliver results, and shape the future * Strong communication skills: capable of presenting complicated and controversial findings to commercial leadership * Therapeutic area experience * Managerial experience * Sales and marketing experience * Excellent oral, written and presentation skills with ability to explain complex concepts clearly to a variety of audiences, including senior management * Ability to work collaboratively in team-based environment * Ability to handle multiple responsibilities, priorities, tasks and projects simultaneously Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. ones OR Business questions OR ability actionable and customer BACH_a33d1a even
Nov 04, 2017
Full time
The Business Analysis and Insights (BAI) Sr. Manager drives business performance and efficiency for Amgen Biosimilars in Oncology. BAI Sr. Manager is a trusted, indispensable advisor to the Executive Director of Brand. He or she is a relentless champion of insights-driven strategy, objective, evidence-based decision making, and effective and efficient commercial activity. The BAI Sr. Manager reports to the Business Analysis & Info (BAI) Business Unit Lead. Job Responsibilities include: * Oversee all US BAI activities, including forecasting, primary market research, competitive intelligence and analytics (national and sub-national) * Develop productive relationships commercial leadership to define BAI objectives, budgets and work plans * Lead a cross functional team of BAI staff (competitive intelligence, payer) to produce proactive, actionable customer and market insights * Ensure commercial leadership understands and accounts for key research results and customer and market insights * Lead the forecasting process for franchise and be able to represent the forecast to commercial leadership * Be a strong "devil's advocate", even with senior commercial staff * Lead initiatives within US BAI to improve existing capabilities and develop new ones * Drives strategic and innovative approaches to key business problems * Ensure that both routine and ad-hoc projects are in compliance with all Amgen SOPs and meet service-level expectations for quality, timeliness, and budget * Manage relationships with external vendors and consultants to enable effective and efficient project execution * Develop productive relationships with cross-functional partners, such as Global BAI, Sales Ops, Global Strategic Sourcing, and Compliance * Conduct primary market research, forecasting & secondary analytics Basic Qualifications: * Doctorate degree and 2 years of analytics experience OR * Master's degree and 4 years of analytics experience OR * Bachelor's degree and 6 years of analytics experience OR * Associate's degree and 10 years of analytics experience OR * High school diploma / GED and 12 years of analytics experience Preferred Qualifications: * Bachelor's degree in marketing, statistics, social, behavioral sciences, or related field of study * 10+ years of experience, including market research, competitive intelligence and/or market analysis * 5+ years of experience managing direct reports * Technical Expertise: Demonstrated ability to translate business questions and needs into actionable research plans and synthesize multiple data sources to answer business questions. * Prior technical forecasting experience or experience managing a forecast * Prior technical experience creating or managing KPI and performance metrics * Innovation: Demonstrated ability to identify and implement new methodologies and data sources to enhance Amgen analytics capabilities * Strong Business Acumen: understands both the markets, brands and broader context (internal and external) of the business. Can translate market research insights and findings into realistic, actionable recommendations * Executive presence: can quickly establish credibility with and influence ED/VP level staff * Strong leadership with a demonstrated ability to build and develop high performing teams, deliver results, and shape the future * Strong communication skills: capable of presenting complicated and controversial findings to commercial leadership * Therapeutic area experience * Managerial experience * Sales and marketing experience * Excellent oral, written and presentation skills with ability to explain complex concepts clearly to a variety of audiences, including senior management * Ability to work collaboratively in team-based environment * Ability to handle multiple responsibilities, priorities, tasks and projects simultaneously Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. ones OR Business questions OR ability actionable and customer BACH_a33d1a even
Awesome opportunity for a full time, permanent medical technologist and a medical lab technician! QUICK FACTS 2 generalist positions: 1 MT and 1 MLT MT: night shift, MLT: variable shift ASCP certification or equivalent preferred New York State license as a MT or MLT is required MT: BS degree in Medical Technology. MLT: AS degree in Medical Lab Technology New grads welcome to apply Very competitive salary Full benefits Located on the Raquette River 2 and a half hours from Syracuse SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. SPECIAL NOTES: Must have a New York State License as a Medical Technologist or Medical Laboratory Technician. (No exceptions) Award-winning hospital is in need of one licensed generalist medical technologist for the night shift and one licensed generalist medical lab technician for variable shifts. ASCP certification or equivalent is preferred but they will accept candidates who are eligible for certification. New grads are welcome to apply. A BS degree in Medical Technology is required for the MT position. An AS degree in Medical Lab Technology is required for the MLT position. They are offering a very competitive salary and full benefits. Downtown Potsdam is laid out along the scenic Raquette River, which flows from the heart of the Adirondacks north to the mighty St. Lawrence. With its distinctive reddish-pink Potsdam sandstone and Victorian architecture, the village offers more than thirty dining locations to choose from, plus specialty shops, accommodations and an independent movie theater. Home to both SUNY Potsdam and Clarkson University, Potsdam is also just down the road from St. Lawrence University and SUNY Canton, located in nearby Canton, N.Y.-making the region a higher education destination. Potsdam also offers one of the state's finest public school systems. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Nov 04, 2017
Full time
Awesome opportunity for a full time, permanent medical technologist and a medical lab technician! QUICK FACTS 2 generalist positions: 1 MT and 1 MLT MT: night shift, MLT: variable shift ASCP certification or equivalent preferred New York State license as a MT or MLT is required MT: BS degree in Medical Technology. MLT: AS degree in Medical Lab Technology New grads welcome to apply Very competitive salary Full benefits Located on the Raquette River 2 and a half hours from Syracuse SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. SPECIAL NOTES: Must have a New York State License as a Medical Technologist or Medical Laboratory Technician. (No exceptions) Award-winning hospital is in need of one licensed generalist medical technologist for the night shift and one licensed generalist medical lab technician for variable shifts. ASCP certification or equivalent is preferred but they will accept candidates who are eligible for certification. New grads are welcome to apply. A BS degree in Medical Technology is required for the MT position. An AS degree in Medical Lab Technology is required for the MLT position. They are offering a very competitive salary and full benefits. Downtown Potsdam is laid out along the scenic Raquette River, which flows from the heart of the Adirondacks north to the mighty St. Lawrence. With its distinctive reddish-pink Potsdam sandstone and Victorian architecture, the village offers more than thirty dining locations to choose from, plus specialty shops, accommodations and an independent movie theater. Home to both SUNY Potsdam and Clarkson University, Potsdam is also just down the road from St. Lawrence University and SUNY Canton, located in nearby Canton, N.Y.-making the region a higher education destination. Potsdam also offers one of the state's finest public school systems. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Vivid Resourcing are committed to equality of opportunity for all applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships or any other characteristic protected by law. Location: Marylebone KEY RESPONSIBILITIES/ACCOUNTABILITIES The post holder is responsible for providing expertise on pharmaceutical drug development and providing support to the Quality Assurance team. They will support departmental investigations such as Deviations and Complaints. They will work closely with the Research and Development department to understand the pharmaceutical properties of the new drugs to be developed and support QA to ensure that appropriate systems of quality are in place. DETAILED RESPONSIBILITIES Provide expert advice and support to the Quality Assurance and Quality Control Teams. Prepares, reviews, updates and completes Quality Management System documentation and validation documentation. Performs reviews of batch records, development reports, or validation documentation for the Investigational medicinal product (IMP) area. Provides regular status updates of current work/projects. Ensuring all investigations which could lead to recall are immediately brought to the attention of the SQAE, QP's and Quality Management Team. Author, review SOP's, validation protocols, file notes, deviations and other quality documents. Ensure training records are kept up to date. Role holder is responsible to maintain cGxP and Health and Safety knowledge relevant to the role. KEY ATTRIBUTES - ESSENTIAL Knowledge: Qualified Pharmacist or Pharmaceutical Science graduate Recent experience in a Pharmaceutical Development/R&D final product GMP Good previous experience in drug development, formulation and toxicology required Skills: Excellent Communication skills High level of numeracy and literacy Excellent attention to detail Attributes and Behaviours: Develops and maintains positive working relationship with the team. Shares ideas and information Ability to meet project deadlines Willingness to assist and coach colleagues as required
Nov 04, 2017
Full time
Vivid Resourcing are committed to equality of opportunity for all applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships or any other characteristic protected by law. Location: Marylebone KEY RESPONSIBILITIES/ACCOUNTABILITIES The post holder is responsible for providing expertise on pharmaceutical drug development and providing support to the Quality Assurance team. They will support departmental investigations such as Deviations and Complaints. They will work closely with the Research and Development department to understand the pharmaceutical properties of the new drugs to be developed and support QA to ensure that appropriate systems of quality are in place. DETAILED RESPONSIBILITIES Provide expert advice and support to the Quality Assurance and Quality Control Teams. Prepares, reviews, updates and completes Quality Management System documentation and validation documentation. Performs reviews of batch records, development reports, or validation documentation for the Investigational medicinal product (IMP) area. Provides regular status updates of current work/projects. Ensuring all investigations which could lead to recall are immediately brought to the attention of the SQAE, QP's and Quality Management Team. Author, review SOP's, validation protocols, file notes, deviations and other quality documents. Ensure training records are kept up to date. Role holder is responsible to maintain cGxP and Health and Safety knowledge relevant to the role. KEY ATTRIBUTES - ESSENTIAL Knowledge: Qualified Pharmacist or Pharmaceutical Science graduate Recent experience in a Pharmaceutical Development/R&D final product GMP Good previous experience in drug development, formulation and toxicology required Skills: Excellent Communication skills High level of numeracy and literacy Excellent attention to detail Attributes and Behaviours: Develops and maintains positive working relationship with the team. Shares ideas and information Ability to meet project deadlines Willingness to assist and coach colleagues as required
Amazing opportunity for two full time permanent medical technologists! QUICK FACTS 2 generalist MT positions Flexible shift BS degree in Medical Technology or equivalent ASCP certification or equivalent preferred New York State license as MT required Sign-on bonus Competitive pay and full benefits Less than two hours from Syracuse Located on the Oswegatchie River SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. SPECIAL NOTES: Must have a New York State License as a Medical Technologist. (No exceptions) Critical access hospital is searching for two generalist medical technologists. They are willing to be flexible on the shift, it can be 5 8's, 4 10's, or 3 12's for evenings or nights. Requires a New York State license as an MT is required. ASCP certification or equivalent is preferred. BS degree in Medical Technology or equivalent is required. They are offering a sign on bonus, competitive pay and benefits. Located less than two hours away from Syracuse, Gouverneur is the gateway to St. Lawrence County. And it is the only town of that name in the entire United States, but that's not the only thing that makes Gouverneur unique. This historic community was founded in 1805, and is nestled between the foothills of the majestic Adirondack Mountains and the bustling Thousands Islands of the St. Lawrence River. The nearby Adirondack Mountains offer high peaks and forested meadows, crisp mountain lakes, hiking trails, down hill skiing and snowmobiling trails. Gouverneur offers the comfort and safety of living in small-town America, knowing you are a short trip away from a wealth of options for work and play. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
Nov 04, 2017
Full time
Amazing opportunity for two full time permanent medical technologists! QUICK FACTS 2 generalist MT positions Flexible shift BS degree in Medical Technology or equivalent ASCP certification or equivalent preferred New York State license as MT required Sign-on bonus Competitive pay and full benefits Less than two hours from Syracuse Located on the Oswegatchie River SPECIAL NOTES: Phlebotomists will NOT be considered for this job. Must have completed a clinical rotation, performing tests in all areas of the lab at a hospital to qualify for a national certification as a Medical Technologist. SPECIAL NOTES: Must have a New York State License as a Medical Technologist. (No exceptions) Critical access hospital is searching for two generalist medical technologists. They are willing to be flexible on the shift, it can be 5 8's, 4 10's, or 3 12's for evenings or nights. Requires a New York State license as an MT is required. ASCP certification or equivalent is preferred. BS degree in Medical Technology or equivalent is required. They are offering a sign on bonus, competitive pay and benefits. Located less than two hours away from Syracuse, Gouverneur is the gateway to St. Lawrence County. And it is the only town of that name in the entire United States, but that's not the only thing that makes Gouverneur unique. This historic community was founded in 1805, and is nestled between the foothills of the majestic Adirondack Mountains and the bustling Thousands Islands of the St. Lawrence River. The nearby Adirondack Mountains offer high peaks and forested meadows, crisp mountain lakes, hiking trails, down hill skiing and snowmobiling trails. Gouverneur offers the comfort and safety of living in small-town America, knowing you are a short trip away from a wealth of options for work and play. To speak NOW with one of our experienced Recruiters about this job or any of our current open jobs, call
The Business Analysis and Insights (BAI) Director leads a team of 3-5 cross-functional analytics professionals to inform pre launch insight generation and drive business performance and efficiency for Amgen's Erenumab. As the leader of the BAI business brand team, the BAI Director is a trusted, indispensable advisor to the Executive Director, Erenumab. He or she is a relentless champion of insights-driven strategy, objective, evidence-based decision making, and effective and efficient commercial activity for Erenumab. The BAI Director will also sit on the leadership team for US BAI and be responsible for driving innovation and building business analytics and intelligence capabilities that give Amgen a competitive advantage. The BAI Director reports to the BAI Business Unit Lead for INBU. Job Responsibilities include: * Oversee all US BAI activities supporting Erenumab, including forecasting, primary market research, competitive intelligence and marketing analytics (national and sub-national) * Develop productive relationships with the Erenumab commercial leadership to define BAI objectives, budgets and work plans. * Manage 2 direct reports but lead a cross functional team of BAI staff (competitive intelligence, forecasting and analytics) to produce proactive, actionable customer and market insights * Ensure commercial leadership understands and accounts for key research results and customer and market insights * Participate and advise in the prelaunch preparedness and forecasting process for the Erenumab franchise and be able to represent the forecast to commercial leadership * Be a strong "devil's advocate", even with senior commercial staff * Lead initiatives within US BAI to improve existing capabilities and develop new ones * Drives strategic and innovative approaches to key business problems * Ensure that both routine and ad-hoc projects are in compliance with all Amgen SOPs and meet service-level expectations for quality, timeliness, and budget * Manage relationships with external vendors and consultants to enable effective and efficient project execution * Develop productive relationships with cross-functional partners, such as Global BAI, Sales Ops, Global Strategic Sourcing, and Compliance * Conduct some key strategic primary market research (~25% of time) * Limited Travel Required Basic Qualifications: * Doctorate degree and 4 years of market research, competitive intelligence and/or market analysis experience OR * Master's degree and 7 years of market research, competitive intelligence and/or market analysis experience OR * Bachelor's degree and 9 years of market research, competitive intelligence and/or market analysis experience Preferred Qualifications: * Technical Expertise: Demonstrated ability to translate business questions and needs into actionable research plans and synthesize multiple data sources to answer business questions * Prior technical forecasting experience or experience managing a forecast * Prior technical experience creating or managing KPI and performance metrics * Innovation: Demonstrated ability to identify and implement new methodologies and data sources to enhance Amgen analytics capabilities * Strong Business Acumen: understands both the markets, brands and broader context (internal and external) of the business. Can translate market research insights and findings into realistic, actionable recommendations * Executive presence: can quickly establish credibility with and influence ED/VP level staff * Strong leadership with a demonstrated ability to build and develop high performing teams, deliver results, and shape the future * Strong communication skills: capable of presenting complicated and controversial findings to commercial leadership * Therapeutic area experience * Managerial experience * Excellent oral, written and presentation skills with ability to explain complex concepts clearly to a variety of audiences, including senior management * Ability to work collaboratively in team-based environment * Skill in handling multiple responsibilities, priorities, tasks and projects simultaneously Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. within strategy plans Develop BACH_a33d1a and
Nov 04, 2017
Full time
The Business Analysis and Insights (BAI) Director leads a team of 3-5 cross-functional analytics professionals to inform pre launch insight generation and drive business performance and efficiency for Amgen's Erenumab. As the leader of the BAI business brand team, the BAI Director is a trusted, indispensable advisor to the Executive Director, Erenumab. He or she is a relentless champion of insights-driven strategy, objective, evidence-based decision making, and effective and efficient commercial activity for Erenumab. The BAI Director will also sit on the leadership team for US BAI and be responsible for driving innovation and building business analytics and intelligence capabilities that give Amgen a competitive advantage. The BAI Director reports to the BAI Business Unit Lead for INBU. Job Responsibilities include: * Oversee all US BAI activities supporting Erenumab, including forecasting, primary market research, competitive intelligence and marketing analytics (national and sub-national) * Develop productive relationships with the Erenumab commercial leadership to define BAI objectives, budgets and work plans. * Manage 2 direct reports but lead a cross functional team of BAI staff (competitive intelligence, forecasting and analytics) to produce proactive, actionable customer and market insights * Ensure commercial leadership understands and accounts for key research results and customer and market insights * Participate and advise in the prelaunch preparedness and forecasting process for the Erenumab franchise and be able to represent the forecast to commercial leadership * Be a strong "devil's advocate", even with senior commercial staff * Lead initiatives within US BAI to improve existing capabilities and develop new ones * Drives strategic and innovative approaches to key business problems * Ensure that both routine and ad-hoc projects are in compliance with all Amgen SOPs and meet service-level expectations for quality, timeliness, and budget * Manage relationships with external vendors and consultants to enable effective and efficient project execution * Develop productive relationships with cross-functional partners, such as Global BAI, Sales Ops, Global Strategic Sourcing, and Compliance * Conduct some key strategic primary market research (~25% of time) * Limited Travel Required Basic Qualifications: * Doctorate degree and 4 years of market research, competitive intelligence and/or market analysis experience OR * Master's degree and 7 years of market research, competitive intelligence and/or market analysis experience OR * Bachelor's degree and 9 years of market research, competitive intelligence and/or market analysis experience Preferred Qualifications: * Technical Expertise: Demonstrated ability to translate business questions and needs into actionable research plans and synthesize multiple data sources to answer business questions * Prior technical forecasting experience or experience managing a forecast * Prior technical experience creating or managing KPI and performance metrics * Innovation: Demonstrated ability to identify and implement new methodologies and data sources to enhance Amgen analytics capabilities * Strong Business Acumen: understands both the markets, brands and broader context (internal and external) of the business. Can translate market research insights and findings into realistic, actionable recommendations * Executive presence: can quickly establish credibility with and influence ED/VP level staff * Strong leadership with a demonstrated ability to build and develop high performing teams, deliver results, and shape the future * Strong communication skills: capable of presenting complicated and controversial findings to commercial leadership * Therapeutic area experience * Managerial experience * Excellent oral, written and presentation skills with ability to explain complex concepts clearly to a variety of audiences, including senior management * Ability to work collaboratively in team-based environment * Skill in handling multiple responsibilities, priorities, tasks and projects simultaneously Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. within strategy plans Develop BACH_a33d1a and
BRÜDER UNTERWEGER GESELLSCHAFT MBH Erste Tiroler Latschenölbrennerei
Austria
DIPL. CHEMIE-VERFAHRENSTECHNIKER(IN) GESUCHT (UNI- ODER FH-ABSCHLUSS) mit Expertise in den Bereichen Destillation & Rektifikation (fraktionierte Destillation unter Vakuum) von organischen Stoffen, diverse Trenntechniken (flüssig-flüssig Extraktionen, präparative Chromatographie etc.) sowie organische Synthese. Schwerpunkt unserer Tätigkeit sind die ätherischen Öle: Destillation, Rektifikation, Qualitätskontrolle, Produktentwicklung Die wöchentliche Normalarbeitszeit beträgt 36 Stunden, Mo-Do (07:30 - 12:00 und 12:30 - 17:00 Uhr) Mehrjährige Praxiserfahrung als Verfahrenstechniker( in) in den Bereichen organische Chemie oder Naturstoffchemie erwünscht Als Mindestgehalt bieten wir Euro 3.400/Monat brutto Überzahlung je nach Qualifikation. Standort: 9911 Thal-Assling (bei Lienz in Osttirol) Kontakt: Herr Stefan Unterweger BRÜDER UNTERWEGER GESELLSCHAFT MBH A-9911 Thal-Assling, Osttirol, Austria Tel.: 0043-(0)4855-8201-0 Fax: 0043-(0)4855-8201-22
Nov 04, 2017
Full time
DIPL. CHEMIE-VERFAHRENSTECHNIKER(IN) GESUCHT (UNI- ODER FH-ABSCHLUSS) mit Expertise in den Bereichen Destillation & Rektifikation (fraktionierte Destillation unter Vakuum) von organischen Stoffen, diverse Trenntechniken (flüssig-flüssig Extraktionen, präparative Chromatographie etc.) sowie organische Synthese. Schwerpunkt unserer Tätigkeit sind die ätherischen Öle: Destillation, Rektifikation, Qualitätskontrolle, Produktentwicklung Die wöchentliche Normalarbeitszeit beträgt 36 Stunden, Mo-Do (07:30 - 12:00 und 12:30 - 17:00 Uhr) Mehrjährige Praxiserfahrung als Verfahrenstechniker( in) in den Bereichen organische Chemie oder Naturstoffchemie erwünscht Als Mindestgehalt bieten wir Euro 3.400/Monat brutto Überzahlung je nach Qualifikation. Standort: 9911 Thal-Assling (bei Lienz in Osttirol) Kontakt: Herr Stefan Unterweger BRÜDER UNTERWEGER GESELLSCHAFT MBH A-9911 Thal-Assling, Osttirol, Austria Tel.: 0043-(0)4855-8201-0 Fax: 0043-(0)4855-8201-22
Die Modelleisenbahn Holding GmbH, eine internationale Unternehmensgruppe mit mehreren Produktionsstandorten im In- und Ausland, Marktführer im Bereich Gleichstrom und Innovationsführer in der Modelleisenbahnbranche mit Hauptsitz in Bergheim bei Salzburg sucht eine/n engagierte/n Das Aufgabengebiet umfasst: Erstellung von einfachen Leiterplattendesigns und deren Unterlagen Fertigung und Testen von Prototypen Technische Abklärung mit Lieferanten und internen Abteilungen Ausarbeitung technischer Unterlagen für Dokumentation Erforderliche Qualifikationen : Abgeschlossene Ausbildung der Fachrichtung Elektronik oder Elektrotechnik Erfahrung mit EAGLE von Vorteil Grundkenntnisse in analoger und digitaler Schaltungstechnik Gute Deutsch- und Englischkenntnisse Gute MS Office-Kenntnisse Sie sind aufgeschlossen, ein/e Teamplayer/in mit hohem Maß an Eigeninitiative, Genauigkeit, Zuverlässigkeit sowie Kreativität und mögen selbstständiges Arbeiten? Dann sind Sie der/die Richtige! Es erwartet Sie ein vielfältiger Aufgabenbereich mit entsprechenden Entwicklungs- und Weiterbildungsmöglichkeiten, leistungsorientierte Bezahlung je nach Qualifikation und Erfahrung sowie ein angenehmes Betriebsklima in einem motiviertem Team. Für diese Position gilt ein Mindestgrundgehalt von EUR 28.000 (Vollzeitbasis) brutto p.a. Weitere Informationen über die Unternehmensgruppe entnehmen Sie bitte den folgenden Websites: , , , , . Wenn Sie Interesse an dieser verantwortungsvollen und abwechslungsreichen Position haben und gerne in einem dynamischen Umfeld arbeiten, dann freuen wir uns über Ihre aussagekräftige Bewerbung mit Angabe Ihrer Gehaltsvorstellungen: Ihre Bewerbung schicken Sie bitte an: Modelleisenbahn GmbH z.Hd. Frau Barbara Gruber Plainbachstraße 4 A-5101 Bergheim per E-Mail unter dem Begriff „Elektronik Entwickler" an
Nov 04, 2017
Full time
Die Modelleisenbahn Holding GmbH, eine internationale Unternehmensgruppe mit mehreren Produktionsstandorten im In- und Ausland, Marktführer im Bereich Gleichstrom und Innovationsführer in der Modelleisenbahnbranche mit Hauptsitz in Bergheim bei Salzburg sucht eine/n engagierte/n Das Aufgabengebiet umfasst: Erstellung von einfachen Leiterplattendesigns und deren Unterlagen Fertigung und Testen von Prototypen Technische Abklärung mit Lieferanten und internen Abteilungen Ausarbeitung technischer Unterlagen für Dokumentation Erforderliche Qualifikationen : Abgeschlossene Ausbildung der Fachrichtung Elektronik oder Elektrotechnik Erfahrung mit EAGLE von Vorteil Grundkenntnisse in analoger und digitaler Schaltungstechnik Gute Deutsch- und Englischkenntnisse Gute MS Office-Kenntnisse Sie sind aufgeschlossen, ein/e Teamplayer/in mit hohem Maß an Eigeninitiative, Genauigkeit, Zuverlässigkeit sowie Kreativität und mögen selbstständiges Arbeiten? Dann sind Sie der/die Richtige! Es erwartet Sie ein vielfältiger Aufgabenbereich mit entsprechenden Entwicklungs- und Weiterbildungsmöglichkeiten, leistungsorientierte Bezahlung je nach Qualifikation und Erfahrung sowie ein angenehmes Betriebsklima in einem motiviertem Team. Für diese Position gilt ein Mindestgrundgehalt von EUR 28.000 (Vollzeitbasis) brutto p.a. Weitere Informationen über die Unternehmensgruppe entnehmen Sie bitte den folgenden Websites: , , , , . Wenn Sie Interesse an dieser verantwortungsvollen und abwechslungsreichen Position haben und gerne in einem dynamischen Umfeld arbeiten, dann freuen wir uns über Ihre aussagekräftige Bewerbung mit Angabe Ihrer Gehaltsvorstellungen: Ihre Bewerbung schicken Sie bitte an: Modelleisenbahn GmbH z.Hd. Frau Barbara Gruber Plainbachstraße 4 A-5101 Bergheim per E-Mail unter dem Begriff „Elektronik Entwickler" an
People have Priority W&H Dentalwerk Bürmoos ist ein zu 100 Prozent österreichisches, familiengeführtes Unternehmen mit rund 1.000 Mitarbeitern und einer Exportquote von 95 Prozent in über 110 Länder. Ein perfekt organisiertes Vertriebsnetz mit 18 Tochterunternehmen und einer Vielzahl an Partnern weltweit garantiert zuverlässige Betreuung und einen ausgezeichneten technischen Service. Aufgabenbereich: > Entwicklung von Medizinprodukten, in Serien überführen und über den Produktlebenszyklus betreuen > Entwicklung von elektronischen Komponenten > Konstruktion von mechanischen Komponenten > Produkte verbessern und weiterentwickeln > Analyse und bearbeiten von Produktreklamationen > Erstellen und aktualisieren der technischen Produktdokumentation Sie bringen mit: > Abgeschlossene technische Ausbildung HTL, Elektrotechnik, Elektronik, Biomedizin mit einschlägiger Berufserfahrung > Selbstständige, zuverlässige und genaue Arbeitsweise > Engagement und Belastbarkeit > Freude und Fähigkeit zur Entwicklung kreativer Lösungen im Team > Bereitschaft zur Weiterbildung > Sehr gute Englischkenntnisse Wir bieten: > Abwechslungsreiches und herausforderndes Aufgabengebiet in einem internationalen Unternehmen > Langfristige Position in einem engagierten Team zum sofortigen Antritt > Einen modernen und gut erreichbaren Arbeitsplatz in Bürmoos bei Salzburg > Monatsbruttogehalt: ab € 2.294,25 abhängig von beruflicher Qualifikation und Erfahrung Haben wir Ihr Interesse geweckt? Dann bewerben Sie sich mit Angabe Ihrer Gehaltsvorstellung bei uns. Entwicklungsingenieur (m/w) Wir suchen zur Verstärkung unseres Entwicklungsbereiches eine/-n W&H Dentalwerk Bürmoos GmbH Personalwesen Ignaz-Glaser-Straße 53, 5111 Bürmoos t + -156 wh.com
Nov 04, 2017
Full time
People have Priority W&H Dentalwerk Bürmoos ist ein zu 100 Prozent österreichisches, familiengeführtes Unternehmen mit rund 1.000 Mitarbeitern und einer Exportquote von 95 Prozent in über 110 Länder. Ein perfekt organisiertes Vertriebsnetz mit 18 Tochterunternehmen und einer Vielzahl an Partnern weltweit garantiert zuverlässige Betreuung und einen ausgezeichneten technischen Service. Aufgabenbereich: > Entwicklung von Medizinprodukten, in Serien überführen und über den Produktlebenszyklus betreuen > Entwicklung von elektronischen Komponenten > Konstruktion von mechanischen Komponenten > Produkte verbessern und weiterentwickeln > Analyse und bearbeiten von Produktreklamationen > Erstellen und aktualisieren der technischen Produktdokumentation Sie bringen mit: > Abgeschlossene technische Ausbildung HTL, Elektrotechnik, Elektronik, Biomedizin mit einschlägiger Berufserfahrung > Selbstständige, zuverlässige und genaue Arbeitsweise > Engagement und Belastbarkeit > Freude und Fähigkeit zur Entwicklung kreativer Lösungen im Team > Bereitschaft zur Weiterbildung > Sehr gute Englischkenntnisse Wir bieten: > Abwechslungsreiches und herausforderndes Aufgabengebiet in einem internationalen Unternehmen > Langfristige Position in einem engagierten Team zum sofortigen Antritt > Einen modernen und gut erreichbaren Arbeitsplatz in Bürmoos bei Salzburg > Monatsbruttogehalt: ab € 2.294,25 abhängig von beruflicher Qualifikation und Erfahrung Haben wir Ihr Interesse geweckt? Dann bewerben Sie sich mit Angabe Ihrer Gehaltsvorstellung bei uns. Entwicklungsingenieur (m/w) Wir suchen zur Verstärkung unseres Entwicklungsbereiches eine/-n W&H Dentalwerk Bürmoos GmbH Personalwesen Ignaz-Glaser-Straße 53, 5111 Bürmoos t + -156 wh.com
Kurtz Holding GmbH & Co. Beteiligungs KG
Kreuzwertheim, Germany
Production needs us. Entwicklungsingenieur/in Hochfrequenztechnik Kennziffer: 1780 Kurtz GmbH | Moulding Machines | 97892 Kreuzwertheim Zur Verstärkung unserer Abteilung Basisentwicklung/Neue Technologien suchen wir zum nächstmöglichen Zeitpunkt in Vollzeit eine/n Entwicklungsingenieur/in Hochfrequenztechnik Ihre Aufgaben: Entwicklung und Optimierung von Hochfrequenztechnologien Stellvertretung des Leiters Neue Technologien im Bereich Hochfrequenztechnologie Betreuung von Prozesssimulationen Durchführung von Testreihen und Parametrisierung der Anlagen Koordination der Entwicklungsprojekte und Betatests beim Kunden vor Ort Koordination von Projekten mit Hochschulen oder externen Partnern Ihre Qualifikationen: Erfolgreich abgeschlossenes Studium als Ingenieur/in Bereich Elektrotechnik oder Diplom Physiker/in Exzellente Kenntnisse im Bereich der Hochfrequenztechnik Erfindergeist und Innovationskompetenz Gutes Englisch in Wort und Schrift Mehrjährige Erfahrung im Bereich Forschung und Entwicklung Gute Kenntnisse im Umgang mit MS Office Wir bieten: Interessante Aufgaben in einer Unternehmensgruppe mit Tradition seit 1779 Einarbeitung und Förderung der persönlichen Kompetenzen im Rahmen unseres modernen Personalentwicklungskonzepts Aktive Förderung der Work-Life-Balance durch unser Programm Attraktiver Arbeitgeber Qualifizierungsmöglichkeiten in der konzerneigenen Hammer- Akademie Attraktive Vergütung mit einer Mitarbeitererfolgsbeteiligung Arbeiten zwischen Spessart und Taubertal in einem Gebiet mit hohem Wohn- und Freizeitwert Kurtz Ersa ist ein Technologie- und Zulieferkonzern in Familienbesitz mit über 235-jähriger Tradition. Daher fühlen wir uns verpflichtet, unsere Strategie auf ein langfristiges, gesundes und nachhaltiges Wachstum auszurichten. In unseren drei Geschäftsfeldern Electronics Production Equipment, Metal Components und Moulding Machines werden unter den Marken Kurtz und Ersa Maschinen, Anlagen, Werkzeuge und Komponenten aus Guss und Blech gefertigt. Unsere Kunden sind Global Player wie BMW, Samsung, Siemens, Volkswagen, Knauf oder ZF. Als Technologieführer mit sieben Standorten im In- und Ausland setzen wir immer wieder neue Maßstäbe, um die Produktivität unserer Kunden weiter zu verbessern. Interessiert? Wir freuen uns auf Ihre vollständigen Bewerbungsunterlagen . Kurtz Holding GmbH & Co. Beteiligungs KG Frankenstraße 2 Fragen? Ihr Ansprechpartner: 97892 Kreuzwertheim Joachim Heilmann Human Resources Manager Business-Coach (IHK) Kurtz GmbH MBW Metallbearbeitung Wertheim GmbH
Nov 04, 2017
Full time
Production needs us. Entwicklungsingenieur/in Hochfrequenztechnik Kennziffer: 1780 Kurtz GmbH | Moulding Machines | 97892 Kreuzwertheim Zur Verstärkung unserer Abteilung Basisentwicklung/Neue Technologien suchen wir zum nächstmöglichen Zeitpunkt in Vollzeit eine/n Entwicklungsingenieur/in Hochfrequenztechnik Ihre Aufgaben: Entwicklung und Optimierung von Hochfrequenztechnologien Stellvertretung des Leiters Neue Technologien im Bereich Hochfrequenztechnologie Betreuung von Prozesssimulationen Durchführung von Testreihen und Parametrisierung der Anlagen Koordination der Entwicklungsprojekte und Betatests beim Kunden vor Ort Koordination von Projekten mit Hochschulen oder externen Partnern Ihre Qualifikationen: Erfolgreich abgeschlossenes Studium als Ingenieur/in Bereich Elektrotechnik oder Diplom Physiker/in Exzellente Kenntnisse im Bereich der Hochfrequenztechnik Erfindergeist und Innovationskompetenz Gutes Englisch in Wort und Schrift Mehrjährige Erfahrung im Bereich Forschung und Entwicklung Gute Kenntnisse im Umgang mit MS Office Wir bieten: Interessante Aufgaben in einer Unternehmensgruppe mit Tradition seit 1779 Einarbeitung und Förderung der persönlichen Kompetenzen im Rahmen unseres modernen Personalentwicklungskonzepts Aktive Förderung der Work-Life-Balance durch unser Programm Attraktiver Arbeitgeber Qualifizierungsmöglichkeiten in der konzerneigenen Hammer- Akademie Attraktive Vergütung mit einer Mitarbeitererfolgsbeteiligung Arbeiten zwischen Spessart und Taubertal in einem Gebiet mit hohem Wohn- und Freizeitwert Kurtz Ersa ist ein Technologie- und Zulieferkonzern in Familienbesitz mit über 235-jähriger Tradition. Daher fühlen wir uns verpflichtet, unsere Strategie auf ein langfristiges, gesundes und nachhaltiges Wachstum auszurichten. In unseren drei Geschäftsfeldern Electronics Production Equipment, Metal Components und Moulding Machines werden unter den Marken Kurtz und Ersa Maschinen, Anlagen, Werkzeuge und Komponenten aus Guss und Blech gefertigt. Unsere Kunden sind Global Player wie BMW, Samsung, Siemens, Volkswagen, Knauf oder ZF. Als Technologieführer mit sieben Standorten im In- und Ausland setzen wir immer wieder neue Maßstäbe, um die Produktivität unserer Kunden weiter zu verbessern. Interessiert? Wir freuen uns auf Ihre vollständigen Bewerbungsunterlagen . Kurtz Holding GmbH & Co. Beteiligungs KG Frankenstraße 2 Fragen? Ihr Ansprechpartner: 97892 Kreuzwertheim Joachim Heilmann Human Resources Manager Business-Coach (IHK) Kurtz GmbH MBW Metallbearbeitung Wertheim GmbH
Position Summary The Content Specialist I (Life Science) is responsible for the test development activities for one or more assessment programs. These assessment programs may be traditional large-scale summative assessments, curriculum-embedded and formative assessments, content or item specifications or enterprise products. The Content Specialist I (Life Science) develops a variety of assessment item types according to standards frameworks and other requirements. The Content Specialist I (Life Science) also helps in the development of item specification documents and supplementary materials, as well as facilitates advisory committee meetings. Additional responsibilities include the following: Contribute to conceptualization, specifications, and creation of innovative content and new assessment products, systems, or services. Use databases and technology tools , including in-house authoring systems, to construct, track, and edit items. Work with project managers to adhere to project schedules and communicate with other functional groups when necessary. Effectively manage work in concurrent projects on different schedules. Participate in the development and maintenance of item, test, and project specifications needed to complete a project or contract. Create and refine a wide variety of item types, including multiple-choice, short-answer, constructed-response, and evidence-based response items, as well as technology-enhanced items, modules, and performance tasks, aligned to standards. Develop item-specific scoring guides, distractor rationales, or other supplemental item information. Participate in item writing workshops and other test development-related activities; listen and address concerns of workshop members, clients and/or developers. Provide feedback for item writers. Review colleagues' work and provide feedback. Follow guidelines for presentation and quality of items, sets, and other work products to ensure uniformity of deliverables. Prepare item sets and materials for committee meetings. Facilitate and guide the work of advisory committees. Interpret and use item statistics in the selection of items; complete item selection and test construction according to blueprint and test specifications. Consult with scoring chief readers during benchmarking. Assist with development of assessment guides, brochures, and sample question packets. Work with Psychometricians to develop items to both content and psychometric parameters including adaptive testing banks. Ascertain and study current trends within national and professional groups' content standards and in how children and adults learn. Participate in personal and professional development. Qualifications Bachelor's Degree (in a life science discipline) and a minimum of three (3) years of teaching experience at the middle school or high school level, and experience using technology with students is required. Master's Degree in Education is highly preferred Content Specialists are required to have in-depth knowledge in a specific discipline to successfully develop test activities for assessment programs. Education/Degree coupled with teaching experience must be in Science
Nov 04, 2017
Full time
Position Summary The Content Specialist I (Life Science) is responsible for the test development activities for one or more assessment programs. These assessment programs may be traditional large-scale summative assessments, curriculum-embedded and formative assessments, content or item specifications or enterprise products. The Content Specialist I (Life Science) develops a variety of assessment item types according to standards frameworks and other requirements. The Content Specialist I (Life Science) also helps in the development of item specification documents and supplementary materials, as well as facilitates advisory committee meetings. Additional responsibilities include the following: Contribute to conceptualization, specifications, and creation of innovative content and new assessment products, systems, or services. Use databases and technology tools , including in-house authoring systems, to construct, track, and edit items. Work with project managers to adhere to project schedules and communicate with other functional groups when necessary. Effectively manage work in concurrent projects on different schedules. Participate in the development and maintenance of item, test, and project specifications needed to complete a project or contract. Create and refine a wide variety of item types, including multiple-choice, short-answer, constructed-response, and evidence-based response items, as well as technology-enhanced items, modules, and performance tasks, aligned to standards. Develop item-specific scoring guides, distractor rationales, or other supplemental item information. Participate in item writing workshops and other test development-related activities; listen and address concerns of workshop members, clients and/or developers. Provide feedback for item writers. Review colleagues' work and provide feedback. Follow guidelines for presentation and quality of items, sets, and other work products to ensure uniformity of deliverables. Prepare item sets and materials for committee meetings. Facilitate and guide the work of advisory committees. Interpret and use item statistics in the selection of items; complete item selection and test construction according to blueprint and test specifications. Consult with scoring chief readers during benchmarking. Assist with development of assessment guides, brochures, and sample question packets. Work with Psychometricians to develop items to both content and psychometric parameters including adaptive testing banks. Ascertain and study current trends within national and professional groups' content standards and in how children and adults learn. Participate in personal and professional development. Qualifications Bachelor's Degree (in a life science discipline) and a minimum of three (3) years of teaching experience at the middle school or high school level, and experience using technology with students is required. Master's Degree in Education is highly preferred Content Specialists are required to have in-depth knowledge in a specific discipline to successfully develop test activities for assessment programs. Education/Degree coupled with teaching experience must be in Science
Position Summary Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: The postdoctoral fellow position is for early career scientist trainees to receive a rigorous scientific training at Regeneron under the auspices of a scientist mentor during a 4-year training period. Fellows will be expected to conduct creative exploratory research that results in publishable data within their fellowship period. The program will consist of: • Four years of formal postdoctoral training in a program directed by an award-winning educator • Exposure to the biotechnology industry's most successful and innovative scientists • Opportunities to pursue cutting-edge, creative biomedical research in a prestigious, well- resourced, and highly driven industry environment • Weekly postdoctoral scientist meetings to foster scientific rigor, creative thinking, critical reasoning, and career advancement • Encouragement of scholarly productivity such as publications and conference presentations As part of your Postdoctoral Training Program, you will: • Conduct forward-looking, innovative, and creative research to address a novel scientific question of your choice under the auspices of a scientist mentor • Publish and disseminate data via external conferences and peer-reviewed publications • Assist with mentoring and teaching intern and other more junior trainees • Participate in postdoctoral program activities such as weekly meetings and the annual research conference • Present data internally, including at lab meetings, trainee meetings, and company wide seminars • Provide ongoing reports of research progress to supervisors and program staff Requirements: • Doctoral degree in a relevant discipline • Scientists looking for their first or second postdoctoral training • Superior scientific skills including critical and analytical thinking • Demonstrated publication success as evidenced by peer-reviewed publications • Good written and oral communication skills • Ability to interact dynamically and constructively with scientific peers • Note: occasional travel Application Details: Applications Accepted: October 1, 2017 - December 1, 2017 Letter of recommendation are required. (Please find additional details in online application) Applications received after December 1, 2017 may not be considered. Following the close date, please allow 3-4 months for review and interviews. Targeted Start Date: July 2018 If you have an issue submitting or any questions, please email: . This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.
Nov 04, 2017
Full time
Position Summary Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: The postdoctoral fellow position is for early career scientist trainees to receive a rigorous scientific training at Regeneron under the auspices of a scientist mentor during a 4-year training period. Fellows will be expected to conduct creative exploratory research that results in publishable data within their fellowship period. The program will consist of: • Four years of formal postdoctoral training in a program directed by an award-winning educator • Exposure to the biotechnology industry's most successful and innovative scientists • Opportunities to pursue cutting-edge, creative biomedical research in a prestigious, well- resourced, and highly driven industry environment • Weekly postdoctoral scientist meetings to foster scientific rigor, creative thinking, critical reasoning, and career advancement • Encouragement of scholarly productivity such as publications and conference presentations As part of your Postdoctoral Training Program, you will: • Conduct forward-looking, innovative, and creative research to address a novel scientific question of your choice under the auspices of a scientist mentor • Publish and disseminate data via external conferences and peer-reviewed publications • Assist with mentoring and teaching intern and other more junior trainees • Participate in postdoctoral program activities such as weekly meetings and the annual research conference • Present data internally, including at lab meetings, trainee meetings, and company wide seminars • Provide ongoing reports of research progress to supervisors and program staff Requirements: • Doctoral degree in a relevant discipline • Scientists looking for their first or second postdoctoral training • Superior scientific skills including critical and analytical thinking • Demonstrated publication success as evidenced by peer-reviewed publications • Good written and oral communication skills • Ability to interact dynamically and constructively with scientific peers • Note: occasional travel Application Details: Applications Accepted: October 1, 2017 - December 1, 2017 Letter of recommendation are required. (Please find additional details in online application) Applications received after December 1, 2017 may not be considered. Following the close date, please allow 3-4 months for review and interviews. Targeted Start Date: July 2018 If you have an issue submitting or any questions, please email: . This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.
Position Summary The Regeneron Genetics Center (RGC) is a wholly-owned subsidiary of the Company, whose goals are to apply large scale human genetics to identify new drug targets and to guide the development of therapeutics programs and precision medicine. Building upon Regeneron's strengths in mouse genetics and genetics-driven drug discovery and development, the RGC specializes in ultra-high-throughput exome sequencing, large scale informatics and data analysis encompassing genomics and electronic health records, and translating genetic discoveries into new biology and drug discovery opportunities. The RGC leverages multiple approaches including large population based studies, Mendelian genetics and family based studies, founder population genetics, and large-scale disease focused projects and has developed a network of over 50 collaborations with research organizations around the world. Including some of the largest sequencing studies in the world, such as the DiscovEHR study in collaboration with Geisinger Health System, and an initiative to sequence 500,000 participants with the UK Biobank, the RGC has built one of the largest human genetics databases, including sequence data from over several hundred thousand participants and rapidly growing. Our interests encompass a breadth of different areas across all therapeutic areas and the RGC is highly integrated into all facets of research and development at Regeneron. Program goals include target discovery, indication discovery, and patient-disease stratification. Objectives include advancing basic science around the world through public sharing of discoveries, providing clinically-valuable insights to physicians and providers of collaborating health-care systems, improving patient outcomes, and identifying novel targets for drug development. Summary: The postdoctoral fellow position is for early career scientist trainees to receive a rigorous scientific training at the Regeneron Genetics Center under the auspices of a scientist mentor during a 4-year training period. Fellows will be expected to conduct creative exploratory research that results in publishable data within their fellowship period. The program will consist of: • Four years of formal postdoctoral training in a program directed by an award-winning educator • Exposure to the biotechnology industry's most successful and innovative scientists • Opportunities to pursue cutting-edge, creative biomedical research in a prestigious, well- resourced, and highly driven industry environment • Weekly postdoctoral scientist meetings to foster scientific rigor, creative thinking, critical reasoning, and career advancement • Encouragement of scholarly productivity such as publications and conference presentations As part of your Postdoctoral Training Program, you will: • Conduct forward-looking, innovative, and creative research to address a novel scientific question of your choice under the auspices of a scientist mentor • Publish and disseminate data via external conferences and peer-reviewed publications • Assist with mentoring and teaching intern and other more junior trainees • Participate in postdoctoral program activities such as weekly meetings and the annual research conference • Present data internally, including at lab meetings, trainee meetings, and company wide seminars • Provide ongoing reports of research progress to supervisors and program staff Education, training, experience: Requirements: • Doctoral degree in a relevant discipline • Scientists looking for their first or second postdoctoral training • Superior scientific skills including critical and analytical thinking • Demonstrated publication success as evidenced by peer-reviewed publications • Good written and oral communication skills • Ability to interact dynamically and constructively with scientific peers • Note: occasional travel Application Details: Applications Accepted: October 1, 2017 - December 1, 2017 Letter of recommendation are required. (Please find additional details in online application) Applications received after December 1, 2017 may not be considered. Following the close date, please allow 3-4 months for review and interviews. Targeted Start Date: July 2018 If you have an issue submitting or any questions, please email:
Nov 04, 2017
Full time
Position Summary The Regeneron Genetics Center (RGC) is a wholly-owned subsidiary of the Company, whose goals are to apply large scale human genetics to identify new drug targets and to guide the development of therapeutics programs and precision medicine. Building upon Regeneron's strengths in mouse genetics and genetics-driven drug discovery and development, the RGC specializes in ultra-high-throughput exome sequencing, large scale informatics and data analysis encompassing genomics and electronic health records, and translating genetic discoveries into new biology and drug discovery opportunities. The RGC leverages multiple approaches including large population based studies, Mendelian genetics and family based studies, founder population genetics, and large-scale disease focused projects and has developed a network of over 50 collaborations with research organizations around the world. Including some of the largest sequencing studies in the world, such as the DiscovEHR study in collaboration with Geisinger Health System, and an initiative to sequence 500,000 participants with the UK Biobank, the RGC has built one of the largest human genetics databases, including sequence data from over several hundred thousand participants and rapidly growing. Our interests encompass a breadth of different areas across all therapeutic areas and the RGC is highly integrated into all facets of research and development at Regeneron. Program goals include target discovery, indication discovery, and patient-disease stratification. Objectives include advancing basic science around the world through public sharing of discoveries, providing clinically-valuable insights to physicians and providers of collaborating health-care systems, improving patient outcomes, and identifying novel targets for drug development. Summary: The postdoctoral fellow position is for early career scientist trainees to receive a rigorous scientific training at the Regeneron Genetics Center under the auspices of a scientist mentor during a 4-year training period. Fellows will be expected to conduct creative exploratory research that results in publishable data within their fellowship period. The program will consist of: • Four years of formal postdoctoral training in a program directed by an award-winning educator • Exposure to the biotechnology industry's most successful and innovative scientists • Opportunities to pursue cutting-edge, creative biomedical research in a prestigious, well- resourced, and highly driven industry environment • Weekly postdoctoral scientist meetings to foster scientific rigor, creative thinking, critical reasoning, and career advancement • Encouragement of scholarly productivity such as publications and conference presentations As part of your Postdoctoral Training Program, you will: • Conduct forward-looking, innovative, and creative research to address a novel scientific question of your choice under the auspices of a scientist mentor • Publish and disseminate data via external conferences and peer-reviewed publications • Assist with mentoring and teaching intern and other more junior trainees • Participate in postdoctoral program activities such as weekly meetings and the annual research conference • Present data internally, including at lab meetings, trainee meetings, and company wide seminars • Provide ongoing reports of research progress to supervisors and program staff Education, training, experience: Requirements: • Doctoral degree in a relevant discipline • Scientists looking for their first or second postdoctoral training • Superior scientific skills including critical and analytical thinking • Demonstrated publication success as evidenced by peer-reviewed publications • Good written and oral communication skills • Ability to interact dynamically and constructively with scientific peers • Note: occasional travel Application Details: Applications Accepted: October 1, 2017 - December 1, 2017 Letter of recommendation are required. (Please find additional details in online application) Applications received after December 1, 2017 may not be considered. Following the close date, please allow 3-4 months for review and interviews. Targeted Start Date: July 2018 If you have an issue submitting or any questions, please email:
This position helps to implement and manage organization-wide compliance and risk management activities. Major Areas of responsibility may include, but are not limited to, incident reporting system, compliment and grievance management, compliance, auditing and monitoring of 340B pharmacy contracting, privacy and HIPAA compliance, billing and reimbursement compliance, contract compliance, regulatory and/or legal research, and developing corporate compliance training. REQUIREMENTS: * Bachelor's degree in health care or business field; equivalent combination of related experience and/or education may substitute for degree. * Minimum three years' additional relevant health care experience. * Related experience must be in the fields of medical records, audits, coding, compliance, legal research, HIPAA, Medicare, Medicaid, and/or quality management, or similar field. * Computer experience required; must demonstrate proficiency in word processing, spreadsheets, and database management. * Demonstrated ability to work independently and successfully manage complex projects. and compliance management helps grievance but BACH_a33d1a
Nov 03, 2017
Full time
This position helps to implement and manage organization-wide compliance and risk management activities. Major Areas of responsibility may include, but are not limited to, incident reporting system, compliment and grievance management, compliance, auditing and monitoring of 340B pharmacy contracting, privacy and HIPAA compliance, billing and reimbursement compliance, contract compliance, regulatory and/or legal research, and developing corporate compliance training. REQUIREMENTS: * Bachelor's degree in health care or business field; equivalent combination of related experience and/or education may substitute for degree. * Minimum three years' additional relevant health care experience. * Related experience must be in the fields of medical records, audits, coding, compliance, legal research, HIPAA, Medicare, Medicaid, and/or quality management, or similar field. * Computer experience required; must demonstrate proficiency in word processing, spreadsheets, and database management. * Demonstrated ability to work independently and successfully manage complex projects. and compliance management helps grievance but BACH_a33d1a
PhysicistOPID Administration Job Description Position is responsible for planning and controlling the distribution of radiation given to patients. Minimum Qualifications: Master of Science in Physics, Health Physics, Radiological Physics or Medical Physics. 0-2 years of clinical experience post graduate training. Licensed in Medical Physics or eligible for licensure. Member of the American Association of Physicists in Medicine. Demonstrates commitment to the Partners-in-Caring process by integrating our culture in all internal and external customer interactions; delivers on our brand promise of we advance health through innovation, accountability, empowerment, collaboration, compassion and results while ensuring one Memorial Hermann Principle Accountabilities: Under general direction, plans and controls the distribution of radiation to patients. Plans and implements initial patient radiation dosage specified by physician. Documents radiation treatment information for federal and state requirements. Monitors and maintains the equipment and techniques being used, and maintains records of the equipment for accrediting agencies. Keeps current dosimetry records on the treatment of each patient and in the department charts. Maintains computer records of radiation dosages for evaluation of weekly dosages. Participates in the Medical Radiology and Isotope committee. Ensures safe care to patients adhering to policies, procedures, and standards, within budgetary specifications, including time management, supply management, productivity, and accuracy of practice. Promotes individual professional growth and development by meeting requirements for mandatory/continuing education, skills competency, supports department-based goals which contribute to the success of the organization. Associated topics: astronomical, astronomy, astrophysics, gravitational, heliophysics, nuclear, physics
Nov 03, 2017
Full time
PhysicistOPID Administration Job Description Position is responsible for planning and controlling the distribution of radiation given to patients. Minimum Qualifications: Master of Science in Physics, Health Physics, Radiological Physics or Medical Physics. 0-2 years of clinical experience post graduate training. Licensed in Medical Physics or eligible for licensure. Member of the American Association of Physicists in Medicine. Demonstrates commitment to the Partners-in-Caring process by integrating our culture in all internal and external customer interactions; delivers on our brand promise of we advance health through innovation, accountability, empowerment, collaboration, compassion and results while ensuring one Memorial Hermann Principle Accountabilities: Under general direction, plans and controls the distribution of radiation to patients. Plans and implements initial patient radiation dosage specified by physician. Documents radiation treatment information for federal and state requirements. Monitors and maintains the equipment and techniques being used, and maintains records of the equipment for accrediting agencies. Keeps current dosimetry records on the treatment of each patient and in the department charts. Maintains computer records of radiation dosages for evaluation of weekly dosages. Participates in the Medical Radiology and Isotope committee. Ensures safe care to patients adhering to policies, procedures, and standards, within budgetary specifications, including time management, supply management, productivity, and accuracy of practice. Promotes individual professional growth and development by meeting requirements for mandatory/continuing education, skills competency, supports department-based goals which contribute to the success of the organization. Associated topics: astronomical, astronomy, astrophysics, gravitational, heliophysics, nuclear, physics
Immediate hire, full time position w/benefits, fast paced workplace, clean & sanitize equipment/rooms. Animal handling & care helpful. May train the right individual in advanced skills if aptitude is demonstrated. Must be able to lift 50 lbs. Safety top priority, WK hrs: weekends, holidays w/rotating schedules.
Nov 03, 2017
Full time
Immediate hire, full time position w/benefits, fast paced workplace, clean & sanitize equipment/rooms. Animal handling & care helpful. May train the right individual in advanced skills if aptitude is demonstrated. Must be able to lift 50 lbs. Safety top priority, WK hrs: weekends, holidays w/rotating schedules.
Marian Regional Medical Center
Santa Maria, CA, USA
Overview Marian Regional Medical Center, located in Santa Maria, California, is a technologically advanced, 191-bed facility that provides safe, quality care to the communities it serves. Marian has been a recipient of the Healthgrades Distinguished Hospital Award for Clinical Excellence for four consecutive years, and was also named among the Top 10% in the Nation for Critical Care by Healthgrades. Marian is designated a STEMI Receiving Center in Santa Barbara County, and is designated a Level III Trauma Center by Santa Barbara County's Emergency Medical Services Agency. The facility has achieved prestigious designation as a Primary Stroke Center by the Joint Commission for advanced, comprehensive care for stroke patients. Our cancer care program is accredited as a Comprehensive Community Cancer Center by the American College of Surgeons' Commission on Cancer, and is one of only three programs between Los Angeles and San Francisco to receive an Outstanding Achievement Award. The campus houses the most comprehensive perinatology/ neonatology program on the Central Coast, providing specialized care to the tiniest of patients. Marian is a member of Dignity Health Central Coast, which also includes Arroyo Grande Community Hospital in Arroyo Grande, CA, French Hospital Medical Center in San Luis Obispo, CA, St. John's Regional Medical Center in Oxnard, CA, and St. John's Pleasant Valley in Camarillo, CA. Dignity Health of the Central Coast is an integrated network of top quality hospitals, physicians from the most prestigious medical schools, and comprehensive outpatient services including primary care offices, premier ambulatory surgery centers, technologically-advanced laboratories and imaging centers and a full service home health agency; all recognized for quality, safety and service. Each hospital is supported by an active philanthropic Foundation to help meet the growing health care needs of our communities. Learn more at Responsibilities About This Position In keeping with the Marian Medical Center health care philosophy, the Clinical Laboratory Scientist II is responsible for the prompt, accurate performance of various chemical, microscopic, and bacteriologic tests to obtain data for use in diagnosis and treatment of disease, in accordance with Mission and Laboratory Customer Service Standards. Performs as General Supervisor as defined in CLIA '88 regulations. Rotates shifts, holidays, and weekends as needed. Duties and responsibilities may be added, deleted, or changed at any time at the discretion of management, following written notice. Selection Criteria Three or more years of recent hospital experience as a Clinical Laboratory Scientist or Medical Technologist. Bachelors degree plus one years training in a school of Clinical Laboratory Science approved by the California State Department of Public Health or equivalent. Must possess a valid California license as a Clinical Laboratory Scientist. ASCP registration desirable. Qualifies as a General Supervisor under CLIA 88 regulations. Associated topics: ascp, medical, microbiology, mls, scientist, services, sterile processing technician, technician, technician lab, toxicology
Nov 03, 2017
Full time
Overview Marian Regional Medical Center, located in Santa Maria, California, is a technologically advanced, 191-bed facility that provides safe, quality care to the communities it serves. Marian has been a recipient of the Healthgrades Distinguished Hospital Award for Clinical Excellence for four consecutive years, and was also named among the Top 10% in the Nation for Critical Care by Healthgrades. Marian is designated a STEMI Receiving Center in Santa Barbara County, and is designated a Level III Trauma Center by Santa Barbara County's Emergency Medical Services Agency. The facility has achieved prestigious designation as a Primary Stroke Center by the Joint Commission for advanced, comprehensive care for stroke patients. Our cancer care program is accredited as a Comprehensive Community Cancer Center by the American College of Surgeons' Commission on Cancer, and is one of only three programs between Los Angeles and San Francisco to receive an Outstanding Achievement Award. The campus houses the most comprehensive perinatology/ neonatology program on the Central Coast, providing specialized care to the tiniest of patients. Marian is a member of Dignity Health Central Coast, which also includes Arroyo Grande Community Hospital in Arroyo Grande, CA, French Hospital Medical Center in San Luis Obispo, CA, St. John's Regional Medical Center in Oxnard, CA, and St. John's Pleasant Valley in Camarillo, CA. Dignity Health of the Central Coast is an integrated network of top quality hospitals, physicians from the most prestigious medical schools, and comprehensive outpatient services including primary care offices, premier ambulatory surgery centers, technologically-advanced laboratories and imaging centers and a full service home health agency; all recognized for quality, safety and service. Each hospital is supported by an active philanthropic Foundation to help meet the growing health care needs of our communities. Learn more at Responsibilities About This Position In keeping with the Marian Medical Center health care philosophy, the Clinical Laboratory Scientist II is responsible for the prompt, accurate performance of various chemical, microscopic, and bacteriologic tests to obtain data for use in diagnosis and treatment of disease, in accordance with Mission and Laboratory Customer Service Standards. Performs as General Supervisor as defined in CLIA '88 regulations. Rotates shifts, holidays, and weekends as needed. Duties and responsibilities may be added, deleted, or changed at any time at the discretion of management, following written notice. Selection Criteria Three or more years of recent hospital experience as a Clinical Laboratory Scientist or Medical Technologist. Bachelors degree plus one years training in a school of Clinical Laboratory Science approved by the California State Department of Public Health or equivalent. Must possess a valid California license as a Clinical Laboratory Scientist. ASCP registration desirable. Qualifies as a General Supervisor under CLIA 88 regulations. Associated topics: ascp, medical, microbiology, mls, scientist, services, sterile processing technician, technician, technician lab, toxicology
Harvey Nash IT Recruitment Switzerland
Fribourg, Switzerland
For our client in Fribourg we are looking for a Customer Order and Supply Management specialist for a 6-month contract . Location: Fribourg Workload: 100% Duration: 2017-11-06 till 2018-04-27 Job Description: Order handling for assigned countries from receipt of order till final invoicing in order to secure smooth order processing. Preparation and issue of offers and quotations for assigned countries. Handling of Letters of Credits and Documentary collections. Contact point for customers, distribution centers, plants, suppliers, banks, Area Managers & Controllers as well as forwarders. Consignment handling. Vacation relief for other countries. Tasks: - Receipt of customer orders, review of all terms and conditions, including price and order entry (or review and validation of EDI orders) and order processing according to existing customer protocol/contracts with close follow up to secure on time delivery - Ensure close follow-up on orders until delivery. - Manage blocked orders, delivery dates, backorders and make sure to keep customer informed at all times. - Issue of commercial invoices, proforma-invoices for tenders and quotations, credit notes, commissions and freight invoices (where applicable). - Organize/assist warehouses, DCs and transportation for export of shipments and constant follow-up until delivery to the customer Support S&OP and marketing in prioritizing orders and if required arrange re-positioning between customers (when applicable). - Customer complaint handling. - Establish and maintain Customer parameters in the ERP and on documents (ECP and/or customer protocol/contracts). - Coordinate product and price set-up/updates. Candidate Profile: - Minimum: Commercial apprenticeship or equivalent. - Preferred: Further education in either export or international customer service. - Fluent in writing and speaking in English French and/or German is a plus - Minimum: 3-5 years of experience in an international customer service. For further information please contact Beata Arciszewska: mail: (see below) tel.: (see below)
Nov 03, 2017
Contractor
For our client in Fribourg we are looking for a Customer Order and Supply Management specialist for a 6-month contract . Location: Fribourg Workload: 100% Duration: 2017-11-06 till 2018-04-27 Job Description: Order handling for assigned countries from receipt of order till final invoicing in order to secure smooth order processing. Preparation and issue of offers and quotations for assigned countries. Handling of Letters of Credits and Documentary collections. Contact point for customers, distribution centers, plants, suppliers, banks, Area Managers & Controllers as well as forwarders. Consignment handling. Vacation relief for other countries. Tasks: - Receipt of customer orders, review of all terms and conditions, including price and order entry (or review and validation of EDI orders) and order processing according to existing customer protocol/contracts with close follow up to secure on time delivery - Ensure close follow-up on orders until delivery. - Manage blocked orders, delivery dates, backorders and make sure to keep customer informed at all times. - Issue of commercial invoices, proforma-invoices for tenders and quotations, credit notes, commissions and freight invoices (where applicable). - Organize/assist warehouses, DCs and transportation for export of shipments and constant follow-up until delivery to the customer Support S&OP and marketing in prioritizing orders and if required arrange re-positioning between customers (when applicable). - Customer complaint handling. - Establish and maintain Customer parameters in the ERP and on documents (ECP and/or customer protocol/contracts). - Coordinate product and price set-up/updates. Candidate Profile: - Minimum: Commercial apprenticeship or equivalent. - Preferred: Further education in either export or international customer service. - Fluent in writing and speaking in English French and/or German is a plus - Minimum: 3-5 years of experience in an international customer service. For further information please contact Beata Arciszewska: mail: (see below) tel.: (see below)
As a part of the Executive team at Concord Biosciences, the main focus of this role is to promote Concord Biosciences' Agrochemical Development and expand our client base while fostering strong client relationships. Act as a liaison between external clients and Concord Biosciences' management and operational teams. The primary emphasis of this position will be to oversee the operations of teams that perform environmental fate, plant and animal metabolism, residue and physical chemistry studies. The successful candidate will have an understanding of study designs and the regulator requirements for these areas. The objective will be to complete studies on time, with quality and with excellent communication with the client. The primary measure of the success in in this role will be the achievement of annual revenue targets set by Executive and Business management. Responsiveness and Delivery to Promise will be the watchwords of the professional. This will include timely communications with clients (call-backs with one business day) and a sense of urgency around projects and deliverables. Minimum Bachelor's degree in life sciences PhD is preferred. Minimum of 5-7 years' experience. The requirements listed above are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Nov 03, 2017
Full time
As a part of the Executive team at Concord Biosciences, the main focus of this role is to promote Concord Biosciences' Agrochemical Development and expand our client base while fostering strong client relationships. Act as a liaison between external clients and Concord Biosciences' management and operational teams. The primary emphasis of this position will be to oversee the operations of teams that perform environmental fate, plant and animal metabolism, residue and physical chemistry studies. The successful candidate will have an understanding of study designs and the regulator requirements for these areas. The objective will be to complete studies on time, with quality and with excellent communication with the client. The primary measure of the success in in this role will be the achievement of annual revenue targets set by Executive and Business management. Responsiveness and Delivery to Promise will be the watchwords of the professional. This will include timely communications with clients (call-backs with one business day) and a sense of urgency around projects and deliverables. Minimum Bachelor's degree in life sciences PhD is preferred. Minimum of 5-7 years' experience. The requirements listed above are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
For the Finance department of Elsevier we are looking for a Credit Controller (36 hours) who speaks native German and has good skills in English. The Credit Control Department is responsible for the final part of the O2C (Order to Cash) process. It is the role of this Department to ensure that the aging balance remains as current as possible and any overdue balances are identified and addressed within the terms of the Global Credit Policy. The Credit Risks represented to Elsevier by its customers is also determined by this Department and appropriate controls and procedures are developed to mitigate any losses through bad debt. Tasks As a Credit Controller at Elsevier you are responsible for the collecting debts process of several customers. With the support of your colleagues you ensure that the payments are made within the terms of the agreement of sale. You also determine requests to extend terms of payment with the support of the Senior Credit Controller in line with the Global Credit Policy and Standard Operating Procedures. You will contact customers about invoices and communicate all disputes raised by the customer to the appropriate departments and ensure that a timely resolution is found. Escalate any unresolved issues as per the Global Credit Policy. Requirements We\'re looking for a candidate (native German speaker) with a background in account management and/or a commercial background and affinity with finance. You\'re capable to communicate effectively with people and put pressure on the customer in a polite manner. You are pro active, highly motivated, ambitious and able to work with different systems. Also, you have an eye for detail, and excellent analytical skills. The offer We offer a salary ranging from euro 2,100 - 2,200 gross per month and an efficient and productive work environment. You will be working in an international environment for 36 hours a week. Uiteraard staat deze vacature open voor zowel mannen als vrouwen.
Nov 03, 2017
Full time
For the Finance department of Elsevier we are looking for a Credit Controller (36 hours) who speaks native German and has good skills in English. The Credit Control Department is responsible for the final part of the O2C (Order to Cash) process. It is the role of this Department to ensure that the aging balance remains as current as possible and any overdue balances are identified and addressed within the terms of the Global Credit Policy. The Credit Risks represented to Elsevier by its customers is also determined by this Department and appropriate controls and procedures are developed to mitigate any losses through bad debt. Tasks As a Credit Controller at Elsevier you are responsible for the collecting debts process of several customers. With the support of your colleagues you ensure that the payments are made within the terms of the agreement of sale. You also determine requests to extend terms of payment with the support of the Senior Credit Controller in line with the Global Credit Policy and Standard Operating Procedures. You will contact customers about invoices and communicate all disputes raised by the customer to the appropriate departments and ensure that a timely resolution is found. Escalate any unresolved issues as per the Global Credit Policy. Requirements We\'re looking for a candidate (native German speaker) with a background in account management and/or a commercial background and affinity with finance. You\'re capable to communicate effectively with people and put pressure on the customer in a polite manner. You are pro active, highly motivated, ambitious and able to work with different systems. Also, you have an eye for detail, and excellent analytical skills. The offer We offer a salary ranging from euro 2,100 - 2,200 gross per month and an efficient and productive work environment. You will be working in an international environment for 36 hours a week. Uiteraard staat deze vacature open voor zowel mannen als vrouwen.
People have Priority W&H Dentalwerk Bürmoos ist ein zu 100 Prozent österreichisches, familiengeführtes Unternehmen mit rund 1.000 Mitarbeitern und einer Exportquote von 95 Prozent in über 110 Länder. Ein perfekt organisiertes Vertriebsnetz mit 18 Tochterunternehmen und einer Vielzahl an Partnern weltweit garantiert zuverlässige Betreuung und einen ausgezeichneten technischen Service. Aufgabenbereich: > Entwicklung von Medizinprodukten, in Serien überführen und über den Produktlebenszyklus betreuen > Entwicklung von elektronischen Komponenten > Konstruktion von mechanischen Komponenten > Produkte verbessern und weiterentwickeln > Analyse und bearbeiten von Produktreklamationen > Erstellen und aktualisieren der technischen Produktdokumentation Sie bringen mit: > Abgeschlossene technische Ausbildung HTL, Elektrotechnik, Elektronik, Biomedizin mit einschlägiger Berufserfahrung > Selbstständige, zuverlässige und genaue Arbeitsweise > Engagement und Belastbarkeit > Freude und Fähigkeit zur Entwicklung kreativer Lösungen im Team > Bereitschaft zur Weiterbildung > Sehr gute Englischkenntnisse Wir bieten: > Abwechslungsreiches und herausforderndes Aufgabengebiet in einem internationalen Unternehmen > Langfristige Position in einem engagierten Team zum sofortigen Antritt > Einen modernen und gut erreichbaren Arbeitsplatz in Bürmoos bei Salzburg > Monatsbruttogehalt: ab € 2.294,25 abhängig von beruflicher Qualifikation und Erfahrung Haben wir Ihr Interesse geweckt? Dann bewerben Sie sich mit Angabe Ihrer Gehaltsvorstellung bei uns. Entwicklungsingenieur (m/w) Wir suchen zur Verstärkung unseres Entwicklungsbereiches eine/-n W&H Dentalwerk Bürmoos GmbH Personalwesen Ignaz-Glaser-Straße 53, 5111 Bürmoos t + -156 wh.com
Nov 03, 2017
Full time
People have Priority W&H Dentalwerk Bürmoos ist ein zu 100 Prozent österreichisches, familiengeführtes Unternehmen mit rund 1.000 Mitarbeitern und einer Exportquote von 95 Prozent in über 110 Länder. Ein perfekt organisiertes Vertriebsnetz mit 18 Tochterunternehmen und einer Vielzahl an Partnern weltweit garantiert zuverlässige Betreuung und einen ausgezeichneten technischen Service. Aufgabenbereich: > Entwicklung von Medizinprodukten, in Serien überführen und über den Produktlebenszyklus betreuen > Entwicklung von elektronischen Komponenten > Konstruktion von mechanischen Komponenten > Produkte verbessern und weiterentwickeln > Analyse und bearbeiten von Produktreklamationen > Erstellen und aktualisieren der technischen Produktdokumentation Sie bringen mit: > Abgeschlossene technische Ausbildung HTL, Elektrotechnik, Elektronik, Biomedizin mit einschlägiger Berufserfahrung > Selbstständige, zuverlässige und genaue Arbeitsweise > Engagement und Belastbarkeit > Freude und Fähigkeit zur Entwicklung kreativer Lösungen im Team > Bereitschaft zur Weiterbildung > Sehr gute Englischkenntnisse Wir bieten: > Abwechslungsreiches und herausforderndes Aufgabengebiet in einem internationalen Unternehmen > Langfristige Position in einem engagierten Team zum sofortigen Antritt > Einen modernen und gut erreichbaren Arbeitsplatz in Bürmoos bei Salzburg > Monatsbruttogehalt: ab € 2.294,25 abhängig von beruflicher Qualifikation und Erfahrung Haben wir Ihr Interesse geweckt? Dann bewerben Sie sich mit Angabe Ihrer Gehaltsvorstellung bei uns. Entwicklungsingenieur (m/w) Wir suchen zur Verstärkung unseres Entwicklungsbereiches eine/-n W&H Dentalwerk Bürmoos GmbH Personalwesen Ignaz-Glaser-Straße 53, 5111 Bürmoos t + -156 wh.com
Physicist - Gamma KnifeTMC Hospital Job Description Position is responsible for planning and controlling the distribution of radiation given to patients. Minimum Qualifications: Master of Science in Physics, Health Physics, Radiological Physics or Medical Physics. 0-2 years of clinical experience post graduate training. Licensed in Medical Physics or eligible for licensure. Member of the American Association of Physicists in Medicine. Demonstrates commitment to the Partners-in-Caring process by integrating our culture in all internal and external customer interactions; delivers on our brand promise of we advance health through innovation, accountability, empowerment, collaboration, compassion and results while ensuring one Memorial Hermann Principle Accountabilities: Under general direction, plans and controls the distribution of radiation to patients. Plans and implements initial patient radiation dosage specified by physician. Documents radiation treatment information for federal and state requirements. Monitors and maintains the equipment and techniques being used, and maintains records of the equipment for accrediting agencies. Keeps current dosimetry records on the treatment of each patient and in the department charts. Maintains computer records of radiation dosages for evaluation of weekly dosages. Participates in the Medical Radiology and Isotope committee. Ensures safe care to patients adhering to policies, procedures, and standards, within budgetary specifications, including time management, supply management, productivity, and accuracy of practice. Promotes individual professional growth and development by meeting requirements for mandatory/continuing education, skills competency, supports department-based goals which contribute to the success of the organization. MNTR KR Associated topics: astronomical, astronomy, astrophysics, gravitational, heliophysics, nuclear, physics
Nov 03, 2017
Full time
Physicist - Gamma KnifeTMC Hospital Job Description Position is responsible for planning and controlling the distribution of radiation given to patients. Minimum Qualifications: Master of Science in Physics, Health Physics, Radiological Physics or Medical Physics. 0-2 years of clinical experience post graduate training. Licensed in Medical Physics or eligible for licensure. Member of the American Association of Physicists in Medicine. Demonstrates commitment to the Partners-in-Caring process by integrating our culture in all internal and external customer interactions; delivers on our brand promise of we advance health through innovation, accountability, empowerment, collaboration, compassion and results while ensuring one Memorial Hermann Principle Accountabilities: Under general direction, plans and controls the distribution of radiation to patients. Plans and implements initial patient radiation dosage specified by physician. Documents radiation treatment information for federal and state requirements. Monitors and maintains the equipment and techniques being used, and maintains records of the equipment for accrediting agencies. Keeps current dosimetry records on the treatment of each patient and in the department charts. Maintains computer records of radiation dosages for evaluation of weekly dosages. Participates in the Medical Radiology and Isotope committee. Ensures safe care to patients adhering to policies, procedures, and standards, within budgetary specifications, including time management, supply management, productivity, and accuracy of practice. Promotes individual professional growth and development by meeting requirements for mandatory/continuing education, skills competency, supports department-based goals which contribute to the success of the organization. MNTR KR Associated topics: astronomical, astronomy, astrophysics, gravitational, heliophysics, nuclear, physics
KLAMATH TRIBES - HUMAN RESOURCES
Chiloquin, OR 97624, USA
Wildlife Biologist $50,532 - $78,728 Full Benefits Prof.-Mgt., Regular, Full-Time This position is located in Chiloquin. For more info contact: The Klamath Tribes PO Box 436 Chiloquin, OR 97624 www. klamathtribes.org x 190 Category: Science , Keywords: Wildlife Biologist
Nov 03, 2017
Full time
Wildlife Biologist $50,532 - $78,728 Full Benefits Prof.-Mgt., Regular, Full-Time This position is located in Chiloquin. For more info contact: The Klamath Tribes PO Box 436 Chiloquin, OR 97624 www. klamathtribes.org x 190 Category: Science , Keywords: Wildlife Biologist
WolfVision is a leading global developer and manufacturer, of innovative systems for effective presentation, collaboration, and knowledge sharing. Universities such as Harvard, London, and Tokyo, and leading companies such as Apple, Audi and Google, use WolfVision Visualizer systems, and their related communication solutions. The company has its headquarters in Austria, and has subsidiaries in USA, Japan, Singapore, Canada, Dubai, and the United Kingdom. Senior Embedded Linux Developer (m/f) As a team member with responsibility for a project, you will independently develop complete embedded systems from the concept stage through to series production. In addition you will support the existing electronics team in the maintenance and further development of firmware for our current product range. Requirements: Development and maintenance of board support packages and device drivers Setup and maintenance of development environments Development of user space applications Programming of microcontrollers in C You have a technical education (university, polytechnic, technical college) in electronics, plus several years experience. You have good knowledge of both the C programming language, and the Linux operating system. Desirable personal attributes include creativity, initiative, flexibility, and motivation, and you should also enjoy working as part of a team. We value a systematic and structured way of working, as well as some negotiating skills for dealing with external partners and suppliers. Knowledge of English is essential. We offer an interesting and challenging position, with a high degree of responsibility, plus performancerelated remuneration. We work in an attractive environment with a pleasant working atmosphere. We look forward to receiving your application! Place of work: Klaus, Austria WolfVision GmbH Oberes Ried 14 | 6833 Klaus Tel:
Nov 03, 2017
Full time
WolfVision is a leading global developer and manufacturer, of innovative systems for effective presentation, collaboration, and knowledge sharing. Universities such as Harvard, London, and Tokyo, and leading companies such as Apple, Audi and Google, use WolfVision Visualizer systems, and their related communication solutions. The company has its headquarters in Austria, and has subsidiaries in USA, Japan, Singapore, Canada, Dubai, and the United Kingdom. Senior Embedded Linux Developer (m/f) As a team member with responsibility for a project, you will independently develop complete embedded systems from the concept stage through to series production. In addition you will support the existing electronics team in the maintenance and further development of firmware for our current product range. Requirements: Development and maintenance of board support packages and device drivers Setup and maintenance of development environments Development of user space applications Programming of microcontrollers in C You have a technical education (university, polytechnic, technical college) in electronics, plus several years experience. You have good knowledge of both the C programming language, and the Linux operating system. Desirable personal attributes include creativity, initiative, flexibility, and motivation, and you should also enjoy working as part of a team. We value a systematic and structured way of working, as well as some negotiating skills for dealing with external partners and suppliers. Knowledge of English is essential. We offer an interesting and challenging position, with a high degree of responsibility, plus performancerelated remuneration. We work in an attractive environment with a pleasant working atmosphere. We look forward to receiving your application! Place of work: Klaus, Austria WolfVision GmbH Oberes Ried 14 | 6833 Klaus Tel:
Alliance Scientific Solutions has partnered with a world leading manufacturer and distributor of snack foods. We are currently seeking a Senior Food Technician for one of their officers located in Burlington, Iowa. As a Senior Food Technician you will be required to innovate, develop, and manage new product implementations. Responsibilities: Develop, plan, manage and execute the steps and stages for our clients product formulation. Accurately set up and launch new products ensuring NLEA and other legal and regulatory compliance. Work with the technical processing team to execute production of new products. Maintain accurate and effective research and development records, documentation, and version control of new formulation, seasoning, and raw material evaluation. Coordinate with QA department to build, manage and maintain processes that ensure 100% packaging and nutritional declaration accuracy. Create new product bases and seasonings and conduct proof of concept work. Ability to manage others. Understands seasonings and pairing flavors. Product alterations based off feedback from sales and R&D. Qualifications: Four year degree in food science or a closely related field. 5-7 years experience in a similar role in the food industry. Knowledge of the applicable regulatory environment.
Nov 02, 2017
Full time
Alliance Scientific Solutions has partnered with a world leading manufacturer and distributor of snack foods. We are currently seeking a Senior Food Technician for one of their officers located in Burlington, Iowa. As a Senior Food Technician you will be required to innovate, develop, and manage new product implementations. Responsibilities: Develop, plan, manage and execute the steps and stages for our clients product formulation. Accurately set up and launch new products ensuring NLEA and other legal and regulatory compliance. Work with the technical processing team to execute production of new products. Maintain accurate and effective research and development records, documentation, and version control of new formulation, seasoning, and raw material evaluation. Coordinate with QA department to build, manage and maintain processes that ensure 100% packaging and nutritional declaration accuracy. Create new product bases and seasonings and conduct proof of concept work. Ability to manage others. Understands seasonings and pairing flavors. Product alterations based off feedback from sales and R&D. Qualifications: Four year degree in food science or a closely related field. 5-7 years experience in a similar role in the food industry. Knowledge of the applicable regulatory environment.
RM IT Professional Resources AG
Basel, Switzerland
Produktionsleiter (w/m) für unseren Kunden aus dem pharmazeutischen Bereich in Base gesucht. Ihre Kenntnisse: Abgeschlossene technische oder kaufmännische Ausbildung mit mehrjähriger Planungserfahrung oder Akademischer Abschluss in betriebswirtschaftlicher, technischer oder naturwissenschaftlicher Fachrichtung 2+ Jahre Erfahrung in Produktionsplanung oder Supply Chain Management Verständnis und Anwendungserfahrung von Planungssystemen (SAP APO, SAP BW, Excel) Sprachen: Deutsch, fliessend in Wort und Schrift, Englisch Kenntnisse sind von Vorteil Ihre Aufgaben: Befolgung der MPS/CRP Prozesse, sowie des Change Control im operationellen Horizont Umsetzung des Produktionsplans ohne Rückstand und ohne Änderungen sowie wöchentliche Abstimmung der Pläne mit dem Betrieb Gewährleistung der Verfügbarkeit sowie Zuteilung der Einsatzkomponenten Garantieren der Vollständigkeit und Richtigkeit der planungsrelevanten Stammdaten Verwaltung der planungsrelevanten Stammdaten im SAP R/3 System Start: per sofort Projektdauer: 12MM+ Ort: Basel, Schweiz Ref.Nr.: BH11863 Klingt das interessant? Fühlen Sie sich angesprochen? Dann machen Sie den nächsten Schritt und senden Sie Ihren Lebenslauf als Word Dokument sowie eine Telefonnummer, unter der wir Sie tagsüber erreichen können. Aufgrund der Schweizer Einschränkungen hinsichtlich der Arbeitserlaubnis können wir nur Bewerbungen von Schweizern, EU-Bürgern und Personen mit Arbeitserlaubnis in Betracht ziehen. Wir bitten um Ihr Verständnis. Neu in der Schweiz? Bei einer erfolgreichen Vermittlung unterstützen wir Sie bei: Bürokratischen Fragen Wohnungssuche Kranken- und Sozialversicherung Arbeitserlaubnis u.v.m.
Nov 02, 2017
Contractor
Produktionsleiter (w/m) für unseren Kunden aus dem pharmazeutischen Bereich in Base gesucht. Ihre Kenntnisse: Abgeschlossene technische oder kaufmännische Ausbildung mit mehrjähriger Planungserfahrung oder Akademischer Abschluss in betriebswirtschaftlicher, technischer oder naturwissenschaftlicher Fachrichtung 2+ Jahre Erfahrung in Produktionsplanung oder Supply Chain Management Verständnis und Anwendungserfahrung von Planungssystemen (SAP APO, SAP BW, Excel) Sprachen: Deutsch, fliessend in Wort und Schrift, Englisch Kenntnisse sind von Vorteil Ihre Aufgaben: Befolgung der MPS/CRP Prozesse, sowie des Change Control im operationellen Horizont Umsetzung des Produktionsplans ohne Rückstand und ohne Änderungen sowie wöchentliche Abstimmung der Pläne mit dem Betrieb Gewährleistung der Verfügbarkeit sowie Zuteilung der Einsatzkomponenten Garantieren der Vollständigkeit und Richtigkeit der planungsrelevanten Stammdaten Verwaltung der planungsrelevanten Stammdaten im SAP R/3 System Start: per sofort Projektdauer: 12MM+ Ort: Basel, Schweiz Ref.Nr.: BH11863 Klingt das interessant? Fühlen Sie sich angesprochen? Dann machen Sie den nächsten Schritt und senden Sie Ihren Lebenslauf als Word Dokument sowie eine Telefonnummer, unter der wir Sie tagsüber erreichen können. Aufgrund der Schweizer Einschränkungen hinsichtlich der Arbeitserlaubnis können wir nur Bewerbungen von Schweizern, EU-Bürgern und Personen mit Arbeitserlaubnis in Betracht ziehen. Wir bitten um Ihr Verständnis. Neu in der Schweiz? Bei einer erfolgreichen Vermittlung unterstützen wir Sie bei: Bürokratischen Fragen Wohnungssuche Kranken- und Sozialversicherung Arbeitserlaubnis u.v.m.
R&D ANALYSTS II in Mayfield Village, OH area. Develop Next Generation insurance product, analysis of companywide product performance & resolution of national policy issues; research new ideas to improve product offerings; develop Project plans; retrieve and verify data from various sources; develop queries & create programs using SAS &/or SQL; work w/ MBI or other reporting tools. Send resume to Progressive Casualty Insurance Company, 6300 Wilson Mills Rd.,Mayfield Village, OH 44143. N72A - CB Category: Science , Keywords: R&D Analyst
Nov 01, 2017
Full time
R&D ANALYSTS II in Mayfield Village, OH area. Develop Next Generation insurance product, analysis of companywide product performance & resolution of national policy issues; research new ideas to improve product offerings; develop Project plans; retrieve and verify data from various sources; develop queries & create programs using SAS &/or SQL; work w/ MBI or other reporting tools. Send resume to Progressive Casualty Insurance Company, 6300 Wilson Mills Rd.,Mayfield Village, OH 44143. N72A - CB Category: Science , Keywords: R&D Analyst
This pharmaceutical testing laboratory based in Watford has an opening for 2 Analytical Chemists. The correct candidate must have a Bachelors or Equivalent Degree in Pharmaceutical Science or Chemical Science with a minimum of 1 years hands on industrial experience using a HPLC system (preferably in a GMP environment). Responsibilities - Analysing samples under cGMP environment using analytical techniques and instrumentation, such as Gas Chromatography, High Performance Liquid Chromatography, ION Chromatography, Dissolution and Spectroscopy (infrared and ultraviolet), amongst others. - Interpreting data and adhering to strict guidelines on documentation when recording data. - Reporting scientific results accurately. Using a range of analytical techniques, instrumentation and software. Working collaboratively in cross-functional teams. Get the Recruitment Genius Advantage today. As the UK's largest online recruitment advertising company placing more candidates than anyone else.
Nov 01, 2017
Full time
This pharmaceutical testing laboratory based in Watford has an opening for 2 Analytical Chemists. The correct candidate must have a Bachelors or Equivalent Degree in Pharmaceutical Science or Chemical Science with a minimum of 1 years hands on industrial experience using a HPLC system (preferably in a GMP environment). Responsibilities - Analysing samples under cGMP environment using analytical techniques and instrumentation, such as Gas Chromatography, High Performance Liquid Chromatography, ION Chromatography, Dissolution and Spectroscopy (infrared and ultraviolet), amongst others. - Interpreting data and adhering to strict guidelines on documentation when recording data. - Reporting scientific results accurately. Using a range of analytical techniques, instrumentation and software. Working collaboratively in cross-functional teams. Get the Recruitment Genius Advantage today. As the UK's largest online recruitment advertising company placing more candidates than anyone else.
Red - The Global SAP Solutions Provider
Munich, Germany
SAP Pharmaceutical Industry Experts - Germany - All locations RED's global client; recognised by Gartner as a leader in Management Consulting, Technology Solutions and IT Outsourcing continues to find success. Widely regarded as the most client centric company, leveraging both best practice methodologies alongside tomorrow's technologies in order to drive profitability and innovation throughout industry leading businesses. We are pleased to offer you the opportunity to join our prestigious partner and take advantage of: 10-15% higher salaries than market Training in best practice methodologies and latest technologies Unrivalled career development program An environment best described as pragmatic & entrepreneurial A profound expertise in Pharmaceutical Industry which is recognised and harnessed by 8 of the top 10 Global Pharma Companies. Your responsibilities: Active participation in SAP implementations on major Pharmaceutical projects. Strengthen and develop the German Life Sciences vertical (market positioning, service development, project and team management,) in close alignment with the global Life Sciences units Responsibility for business development and pre-sales activities, including the creation of proposals, preparation and facilitation of sales presentations and contract negotiations Design and execute complex transformation programs, covering all aspects from strategic road-map design to organisational design, process definition and system integration Build and manage sustainable client relationships and act as a trusted advisor on C-level Your qualifications All levels (Consultant to Managing Consultant). Higher education degree in Economics, Information Technology or equivalent Professional consulting experience from BigFour to specialist boutiques. Proven track record in end-to-end transformation programs in the life sciences space, including stakeholder and change management Strong SAP background (Any area: Logistics, Finance, CRM, SCM, BI etc...) Knowledge regarding the specifics of the life sciences industry related to Core Operations, Research & Development (incl. Clinical Trials) and Marketing & Sales Well-founded project management (at Senior Consultant & Manager level) or team lead experience in an international work environment as well as outstanding communication and presentation skills Willingness to travel and an excellent command of German and English
Nov 01, 2017
Full time
SAP Pharmaceutical Industry Experts - Germany - All locations RED's global client; recognised by Gartner as a leader in Management Consulting, Technology Solutions and IT Outsourcing continues to find success. Widely regarded as the most client centric company, leveraging both best practice methodologies alongside tomorrow's technologies in order to drive profitability and innovation throughout industry leading businesses. We are pleased to offer you the opportunity to join our prestigious partner and take advantage of: 10-15% higher salaries than market Training in best practice methodologies and latest technologies Unrivalled career development program An environment best described as pragmatic & entrepreneurial A profound expertise in Pharmaceutical Industry which is recognised and harnessed by 8 of the top 10 Global Pharma Companies. Your responsibilities: Active participation in SAP implementations on major Pharmaceutical projects. Strengthen and develop the German Life Sciences vertical (market positioning, service development, project and team management,) in close alignment with the global Life Sciences units Responsibility for business development and pre-sales activities, including the creation of proposals, preparation and facilitation of sales presentations and contract negotiations Design and execute complex transformation programs, covering all aspects from strategic road-map design to organisational design, process definition and system integration Build and manage sustainable client relationships and act as a trusted advisor on C-level Your qualifications All levels (Consultant to Managing Consultant). Higher education degree in Economics, Information Technology or equivalent Professional consulting experience from BigFour to specialist boutiques. Proven track record in end-to-end transformation programs in the life sciences space, including stakeholder and change management Strong SAP background (Any area: Logistics, Finance, CRM, SCM, BI etc...) Knowledge regarding the specifics of the life sciences industry related to Core Operations, Research & Development (incl. Clinical Trials) and Marketing & Sales Well-founded project management (at Senior Consultant & Manager level) or team lead experience in an international work environment as well as outstanding communication and presentation skills Willingness to travel and an excellent command of German and English
The Henry M. Jackson Foundation
Frederick, MD, USA
The Henry M. Jackson Foundation for the Advancement of Military Medicine (HJF) is looking for junior and senior scientists to join the U.S. Army Medical Research and Materiel Command's Biotechnology High Performance Computing Software Applications Institute (BHSAI) [] located in Frederick, Maryland. HJF provides scientific, technical, and programmatic support services to the BHSAI. This opening is for dynamic research scientists interested in working in multiple cross-disciplinary research projects. The Computational Biologist is responsible for advancing scientific knowledge by developing and applying their knowledge to original research problems in Military Medicine. The Research Scientist will apply their experiences in the collection, analysis, integration, and modeling of large datasets using computational biology and systems biology methods to provide key biological and physiological insights in the field of immunology and vaccine research. The successful candidate will support and drive research in computational immunology and vaccine design. The candidate will work closely with multiple research teams to design, develop, and implement tools, systems, and methods to use complex multi-platform datasets to advance our understanding of the biology of infectious diseases and vaccines. The candidate is expected to have the following major duties and responsibilities: Perform expert computational research in immunology and infectious diseases and establish scientific hypotheses that can be addressed using computational methods Carry out data analysis and modeling activities through the design and delivery of novel algorithms, tools, and techniques using genomic, transcriptomic, proteomic, flow cytometry, and biological screening assays Support the development of databases, software, and user-interfaces that implement newly developed algorithms or methods Provide expert advice on computational biology tools, experimental design, data analysis, and data interpretation Present research results at scientific conferences and prepare manuscripts for publication in peer-reviewed journals Actively identify and pursue opportunities to collaborate externally in support of the BHSAI's technical and scientific goals with experts and collaborators Minimum Education/Training Requirements: Ph.D. in Bioinformatics, Computational Biology, Systems Biology, or closely related field. Depending on seniority level and experience, the candidate is expected to have the following qualifications: Solid knowledge of informatics tools and visualization/data mining packages and a proven aptitude for optimally adapting them to specific problems Proficiency in common database/programming/scripting languages (e.g., SQL, R, Python, Perl, Java, MATLAB, C++) and their application in biomedical research First-hand experience in analyzing and interpreting large and complex data sets and a familiarity with common data types Excellent writing and oral communication skills Proven track-record of publishing relevant bioinformatics or systems biology results in peer-reviewed journals Working knowledge of biostatistics including significance testing, power analysis, and boot-strapping methods Demonstrated scientific knowledge of cell biology, molecular biology, and/or immunology Minimum Experience: 2-4 years of experience preferred. Previous computational biology experience is a MUST HAVE. PLEASE ONLY APPLY IF YOU HAVE PROVEN COMPUTATIONAL BIOLOGY EXPERIENCE. The candidate is expected to simultaneously work on multiple projects, involving a diverse and interdisciplinary team of scientists across multiple laboratories. Background Requirement: Candidates must be eligible to receive a Public Trust clearance. Foreign nationals are welcome to apply. U.S. citizenship or permanent resident status is not required. However, a background requirement is that the employee must have lived in the US three consecutive years out of the past five years. HJF is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Nov 01, 2017
Full time
The Henry M. Jackson Foundation for the Advancement of Military Medicine (HJF) is looking for junior and senior scientists to join the U.S. Army Medical Research and Materiel Command's Biotechnology High Performance Computing Software Applications Institute (BHSAI) [] located in Frederick, Maryland. HJF provides scientific, technical, and programmatic support services to the BHSAI. This opening is for dynamic research scientists interested in working in multiple cross-disciplinary research projects. The Computational Biologist is responsible for advancing scientific knowledge by developing and applying their knowledge to original research problems in Military Medicine. The Research Scientist will apply their experiences in the collection, analysis, integration, and modeling of large datasets using computational biology and systems biology methods to provide key biological and physiological insights in the field of immunology and vaccine research. The successful candidate will support and drive research in computational immunology and vaccine design. The candidate will work closely with multiple research teams to design, develop, and implement tools, systems, and methods to use complex multi-platform datasets to advance our understanding of the biology of infectious diseases and vaccines. The candidate is expected to have the following major duties and responsibilities: Perform expert computational research in immunology and infectious diseases and establish scientific hypotheses that can be addressed using computational methods Carry out data analysis and modeling activities through the design and delivery of novel algorithms, tools, and techniques using genomic, transcriptomic, proteomic, flow cytometry, and biological screening assays Support the development of databases, software, and user-interfaces that implement newly developed algorithms or methods Provide expert advice on computational biology tools, experimental design, data analysis, and data interpretation Present research results at scientific conferences and prepare manuscripts for publication in peer-reviewed journals Actively identify and pursue opportunities to collaborate externally in support of the BHSAI's technical and scientific goals with experts and collaborators Minimum Education/Training Requirements: Ph.D. in Bioinformatics, Computational Biology, Systems Biology, or closely related field. Depending on seniority level and experience, the candidate is expected to have the following qualifications: Solid knowledge of informatics tools and visualization/data mining packages and a proven aptitude for optimally adapting them to specific problems Proficiency in common database/programming/scripting languages (e.g., SQL, R, Python, Perl, Java, MATLAB, C++) and their application in biomedical research First-hand experience in analyzing and interpreting large and complex data sets and a familiarity with common data types Excellent writing and oral communication skills Proven track-record of publishing relevant bioinformatics or systems biology results in peer-reviewed journals Working knowledge of biostatistics including significance testing, power analysis, and boot-strapping methods Demonstrated scientific knowledge of cell biology, molecular biology, and/or immunology Minimum Experience: 2-4 years of experience preferred. Previous computational biology experience is a MUST HAVE. PLEASE ONLY APPLY IF YOU HAVE PROVEN COMPUTATIONAL BIOLOGY EXPERIENCE. The candidate is expected to simultaneously work on multiple projects, involving a diverse and interdisciplinary team of scientists across multiple laboratories. Background Requirement: Candidates must be eligible to receive a Public Trust clearance. Foreign nationals are welcome to apply. U.S. citizenship or permanent resident status is not required. However, a background requirement is that the employee must have lived in the US three consecutive years out of the past five years. HJF is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
University Hospitals
North Royalton, OH 44133, USA
Processes tissue samples by embedding, sectioning and staining slides for histological diagnosis. Education/Expertise: High school diploma Graduate of histology program Required Credentials, Licensure or Certification (i.e. RN, RRT): Certification as a Histotechnician (HT) or eligible Equal Opportunity Employer - minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity. Associated topics: antibody, biopharmaceutical, diet, dietetic, dietician, food, health, histotechnologist, microbiology, nephrology
Oct 31, 2017
Full time
Processes tissue samples by embedding, sectioning and staining slides for histological diagnosis. Education/Expertise: High school diploma Graduate of histology program Required Credentials, Licensure or Certification (i.e. RN, RRT): Certification as a Histotechnician (HT) or eligible Equal Opportunity Employer - minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity. Associated topics: antibody, biopharmaceutical, diet, dietetic, dietician, food, health, histotechnologist, microbiology, nephrology
Michael Bailey Associates - Munich
Basel, Switzerland
We are currently looking for a Process Validation Expert to validate biotech drug products. For this role you will need a thorough understanding of manufacturing processes for both upstream (USP) and downstream processing (DSP) as well as in regulatory affairs (S25). This is a 9 month contract role, with possibilities of extension highly likely. Job description Please note that no sponsorship is available, thus candidates will have to have no restrictions on their eligibility to work in Switzerland. Responsibilities: You will write process validation reports which will serve as source documents for a BLA (Biologics License Application). Author process validation reports for biotech drug substance processes (Upstream and Downstream). Analyze and evaluate process data from executed validation studies. Basic Requirements: MSc or BSc. in Chemistry, Pharmacy, (Bio-)Chemical Engineering or Pharmaceutical Technology. Thorough understanding of biotech manufacturing processes and related process equipment (USP and DSP). Experience in process validation. Expertise in writing technical reports in English Experience in regulatory affairs particular in writing module S25. English & German fluent. Please send CVs or call. Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Oct 31, 2017
Contractor
We are currently looking for a Process Validation Expert to validate biotech drug products. For this role you will need a thorough understanding of manufacturing processes for both upstream (USP) and downstream processing (DSP) as well as in regulatory affairs (S25). This is a 9 month contract role, with possibilities of extension highly likely. Job description Please note that no sponsorship is available, thus candidates will have to have no restrictions on their eligibility to work in Switzerland. Responsibilities: You will write process validation reports which will serve as source documents for a BLA (Biologics License Application). Author process validation reports for biotech drug substance processes (Upstream and Downstream). Analyze and evaluate process data from executed validation studies. Basic Requirements: MSc or BSc. in Chemistry, Pharmacy, (Bio-)Chemical Engineering or Pharmaceutical Technology. Thorough understanding of biotech manufacturing processes and related process equipment (USP and DSP). Experience in process validation. Expertise in writing technical reports in English Experience in regulatory affairs particular in writing module S25. English & German fluent. Please send CVs or call. Michael Bailey International is acting as an Employment Business in relation to this vacancy.
American Consumer Panels® is a consulting firm that specializes in product testing and product development work. We design and conduct In-Home Usage Testing (IHUT) locally and nationally to provide actual user feedback to companies and market research firms to evaluate products, packaging, related product instructions and more. We leverage our network of private panels (In-Home Usage Testers) to provide product testers to companies for evaluating the in-home experience with a wide variety of products to ensure proper product certification and greater market access. Please note that although this job can be done from home 95% of the time, very occasionally In-Home Product Testers may be asked to visit the client's office, laboratory, store, warehouse or factory for training or meetings (visits are local and scheduled at no more than 20 minutes drive from the In-Home Usage Tester address). These optional visits are also paid by the hour. During your application process, we will determine your consumer profile and establish what products would be suitable for you to test according to your demographics, lifestyle, consumer behavior, skills, hobbies and ability. Research questionnaires are used to identify and target certain types of consumers, to ensure the right participants are engaged and to achieve the representative sample needed. Job candidates for In-Home Usage Testing are also screened to meet the client's needs for the project to ensure that the product is one that they qualify to test and that they have a balance of demographics and attitudes. Participation in these product testing and consumer panels is always free, secure and private. In-Home Usage Testing is a quick, easy and fun way to make extra cash by telling big brands what you think about their upcoming products and services in the American market. Main duties: * Sign and return non-disclosure agreements before the product to be tested is shipped. Individuals who complete the required documents will have the products sent to their homes. * Once the product is received for In-Home Usage Test (IHUT), the Product Tester must take care of the product being tested and use it responsibly. * Read and strictly follow the In-Home Usage Test Daily Schedule provided with each product testing project. In-Home Usage Test Daily Schedules may include tasks to do such as: unpacking, reading instructions, journal entries, online or mobile feedback, usage of product for certain amount of time, writing reviews, taking pictures, etc. * Properly document In-Home Usage Test as instructed in the In-Home Usage Test Daily Schedule. Types of documentation commonly used for In-Home Usage Tests are snapshots, audio recordings, videos and Product Journals. * Attend Skype meetings or conference call meetings with Account Managers, Brand Managers, Research Managers, Product Managers or small business owners to offer ongoing product usage feedback. These short virtual meetings may take place 2-3 times per week and are paid by the hour also. * Some In-Home Usage Tests projects may require participants to use MFour's Mobile In-Home Use Test Technology (cutting edge smartphone technology to capture Point-of-Emotion® insights to gain unparalleled depth of responses). * Paid Product Testing is done from home 95% of the time, but very occasionally paid Product Testers may be asked to visit the client's office, laboratory, store, warehouse or factory for training or meetings. These visits are paid by the hour also. * There are times when the product testing may be discussed in a private chat room that is opened by the market research group. * Write reviews as requested in the In-Home Usage Test Daily Schedule for each project. * Review requirements can vary, however, the standard requirement is a written review, photos of the reviewer with the product and a video review. Requirements: * Great ability to follow precise instructions * Be open to write short reviews, record audio or short video (doesn't have to be perfect), no experience needed * Great attention to detail and curious spirit * Be able to work 15-20 hours per week and commit to a certain routine * Have access to a computer and a reliable internet connection * Have access to a digital camera or cellphone that takes pictures * Be honest and reliable * Good communication skills is an asset * No experience required * High School Diploma * 18 years or older A paid Product Tester position is perfect for those looking for an entry level opportunity or for seasonal work, temporary work or part-time work. The hours are completely flexible and no previous experience is necessary. Our paid Product Testers come from all backgrounds and industries ranging from customer service and sales to administrative assistant. If you are a manager, receptionist, warehouse or factory worker, driver, medical assistant, nurse, cleaner, college student, messenger, maid, teacher, retail associate, salesperson, secretary, server, janitor, cashier, contract worker or intern who is looking for a flexible part time or seasonal job, you should try paid Product Testing to supplement your income. Also if you have been involved in accounting, clerical jobs, marketing, management, security or data entry jobs you may qualify for a paid product tester position. Benefits: * Very competitive salary * Weekly pay * Work around your schedule * Learn about an exciting industry * Telecommute (you can work from home, work or school) * Most of the time you can keep the product tested * An incredible team comprised of motivated and talented individuals and are each to BACH_a33d1a brands a skills entries
Oct 31, 2017
Full time
American Consumer Panels® is a consulting firm that specializes in product testing and product development work. We design and conduct In-Home Usage Testing (IHUT) locally and nationally to provide actual user feedback to companies and market research firms to evaluate products, packaging, related product instructions and more. We leverage our network of private panels (In-Home Usage Testers) to provide product testers to companies for evaluating the in-home experience with a wide variety of products to ensure proper product certification and greater market access. Please note that although this job can be done from home 95% of the time, very occasionally In-Home Product Testers may be asked to visit the client's office, laboratory, store, warehouse or factory for training or meetings (visits are local and scheduled at no more than 20 minutes drive from the In-Home Usage Tester address). These optional visits are also paid by the hour. During your application process, we will determine your consumer profile and establish what products would be suitable for you to test according to your demographics, lifestyle, consumer behavior, skills, hobbies and ability. Research questionnaires are used to identify and target certain types of consumers, to ensure the right participants are engaged and to achieve the representative sample needed. Job candidates for In-Home Usage Testing are also screened to meet the client's needs for the project to ensure that the product is one that they qualify to test and that they have a balance of demographics and attitudes. Participation in these product testing and consumer panels is always free, secure and private. In-Home Usage Testing is a quick, easy and fun way to make extra cash by telling big brands what you think about their upcoming products and services in the American market. Main duties: * Sign and return non-disclosure agreements before the product to be tested is shipped. Individuals who complete the required documents will have the products sent to their homes. * Once the product is received for In-Home Usage Test (IHUT), the Product Tester must take care of the product being tested and use it responsibly. * Read and strictly follow the In-Home Usage Test Daily Schedule provided with each product testing project. In-Home Usage Test Daily Schedules may include tasks to do such as: unpacking, reading instructions, journal entries, online or mobile feedback, usage of product for certain amount of time, writing reviews, taking pictures, etc. * Properly document In-Home Usage Test as instructed in the In-Home Usage Test Daily Schedule. Types of documentation commonly used for In-Home Usage Tests are snapshots, audio recordings, videos and Product Journals. * Attend Skype meetings or conference call meetings with Account Managers, Brand Managers, Research Managers, Product Managers or small business owners to offer ongoing product usage feedback. These short virtual meetings may take place 2-3 times per week and are paid by the hour also. * Some In-Home Usage Tests projects may require participants to use MFour's Mobile In-Home Use Test Technology (cutting edge smartphone technology to capture Point-of-Emotion® insights to gain unparalleled depth of responses). * Paid Product Testing is done from home 95% of the time, but very occasionally paid Product Testers may be asked to visit the client's office, laboratory, store, warehouse or factory for training or meetings. These visits are paid by the hour also. * There are times when the product testing may be discussed in a private chat room that is opened by the market research group. * Write reviews as requested in the In-Home Usage Test Daily Schedule for each project. * Review requirements can vary, however, the standard requirement is a written review, photos of the reviewer with the product and a video review. Requirements: * Great ability to follow precise instructions * Be open to write short reviews, record audio or short video (doesn't have to be perfect), no experience needed * Great attention to detail and curious spirit * Be able to work 15-20 hours per week and commit to a certain routine * Have access to a computer and a reliable internet connection * Have access to a digital camera or cellphone that takes pictures * Be honest and reliable * Good communication skills is an asset * No experience required * High School Diploma * 18 years or older A paid Product Tester position is perfect for those looking for an entry level opportunity or for seasonal work, temporary work or part-time work. The hours are completely flexible and no previous experience is necessary. Our paid Product Testers come from all backgrounds and industries ranging from customer service and sales to administrative assistant. If you are a manager, receptionist, warehouse or factory worker, driver, medical assistant, nurse, cleaner, college student, messenger, maid, teacher, retail associate, salesperson, secretary, server, janitor, cashier, contract worker or intern who is looking for a flexible part time or seasonal job, you should try paid Product Testing to supplement your income. Also if you have been involved in accounting, clerical jobs, marketing, management, security or data entry jobs you may qualify for a paid product tester position. Benefits: * Very competitive salary * Weekly pay * Work around your schedule * Learn about an exciting industry * Telecommute (you can work from home, work or school) * Most of the time you can keep the product tested * An incredible team comprised of motivated and talented individuals and are each to BACH_a33d1a brands a skills entries
Schrack Seconet ist ein österreichisches Hightech-Unternehmen mit Hauptsitz in Wien, Geschäftsstellen in den Bundesländern und Niederlassungen/Partnern in der ganzen Welt. In den Bereichen Brandmelde-, Kommunikations- und Sicherheitssysteme zählen wir zu den führenden Unternehmen des Weltmarktes. Für unsere Entwicklungsabteilung im Headquarter Wien suchen wir Unterstützung. Elektronik-Entwickler (m/w) Ihre Aufgaben EMV-gerechtes Design von Schaltungen im Analog- und Digitalbereich Simulation und Test von Prototypen Durchführung der Entwicklungsprojekte vom Entwurf bis zur Serienreife Unsere Anforderungen Abgeschlossene Ausbildung einer HTL, FH oder TU Mehrjährige Erfahrung in Hard- und Firmwareentwicklung Gute Kenntnisse im Bereich von Analog-, Digital- und Datenübertragungstechnik sowie in hardwarenaher Programmierung z.B. C Wenn Sie Teamgeist besitzen, Kontaktfreudigkeit und Belastbarkeit zu Ihren Stärken zählen, möchten wir Sie gerne kennenlernen. Das monatliche Mindestentgelt (ohne Sonderzahlungen) für diese Tätigkeit beträgt € 3.500,-- brutto, wobei die Bereitschaft zu einer weiteren Überzahlung bei entsprechender Qualifikation und Erfahrung vorhanden ist. Es erwartet Sie eine vielseitige Tätigkeit, ein krisensicherer Arbeitsplatz mit flexiblen Arbeitszeiten, leistungsgerechte Bezahlung und eine ausgezeichnete Unternehmenskultur! Wir freuen uns auf Ihre Bewerbung! Detaillierte schriftliche Bewerbungsunterlagen samt Lebenslauf, Foto und Zeugnissen senden Sie bitte per E-Mail oder Post an: SCHRACK SECONET AG z.H. Frau Barbara Lang 1120 Wien, Eibesbrunnergasse 18
Oct 31, 2017
Full time
Schrack Seconet ist ein österreichisches Hightech-Unternehmen mit Hauptsitz in Wien, Geschäftsstellen in den Bundesländern und Niederlassungen/Partnern in der ganzen Welt. In den Bereichen Brandmelde-, Kommunikations- und Sicherheitssysteme zählen wir zu den führenden Unternehmen des Weltmarktes. Für unsere Entwicklungsabteilung im Headquarter Wien suchen wir Unterstützung. Elektronik-Entwickler (m/w) Ihre Aufgaben EMV-gerechtes Design von Schaltungen im Analog- und Digitalbereich Simulation und Test von Prototypen Durchführung der Entwicklungsprojekte vom Entwurf bis zur Serienreife Unsere Anforderungen Abgeschlossene Ausbildung einer HTL, FH oder TU Mehrjährige Erfahrung in Hard- und Firmwareentwicklung Gute Kenntnisse im Bereich von Analog-, Digital- und Datenübertragungstechnik sowie in hardwarenaher Programmierung z.B. C Wenn Sie Teamgeist besitzen, Kontaktfreudigkeit und Belastbarkeit zu Ihren Stärken zählen, möchten wir Sie gerne kennenlernen. Das monatliche Mindestentgelt (ohne Sonderzahlungen) für diese Tätigkeit beträgt € 3.500,-- brutto, wobei die Bereitschaft zu einer weiteren Überzahlung bei entsprechender Qualifikation und Erfahrung vorhanden ist. Es erwartet Sie eine vielseitige Tätigkeit, ein krisensicherer Arbeitsplatz mit flexiblen Arbeitszeiten, leistungsgerechte Bezahlung und eine ausgezeichnete Unternehmenskultur! Wir freuen uns auf Ihre Bewerbung! Detaillierte schriftliche Bewerbungsunterlagen samt Lebenslauf, Foto und Zeugnissen senden Sie bitte per E-Mail oder Post an: SCHRACK SECONET AG z.H. Frau Barbara Lang 1120 Wien, Eibesbrunnergasse 18
University of California, Riverside
Riverside, CA, USA
Job Description: The Department of Biochemistry at the University of California, Riverside invites applications for a new 9-month faculty position at the Assistant Professor (tenure-track) or early Associate Professor level (tenured) in the general area of physical biochemistry, with a particular emphasis in the application of Cryo-EM to investigate problems of fundamental biological and biomedical importance. The position will build on existing campus strengths in structural biology and related areas of biophysics, including faculty using X-ray crystallography, NMR and single-molecule methods to study DNA repair, epigenetics, regulation of translation and cell signaling. The successful candidate will have a record of original research accomplishments; some experience in grant/fellowship proposal preparation is desirable. S/he will be expected to develop a vigorous, independent, and internationally recognized research program that is able to attract extramural funding; s/he will also develop and teach graduate and undergraduate courses, advise and mentor graduate and undergraduate students, and engage in both campus and professional service activities. A competitive start-up package will be provided, with salary commensurate with education, training and experience. The position is available July 1, 2018. A Ph.D., M.D., or equivalent degree in biochemistry or a related field is required, as well as postdoctoral experience. Interested individuals should submit a cover letter, a full curriculum vitae, a statement of research, a statement of teaching philosophy, and a statement of contributions to diversity. In addition, applicants for the Assistant level position should arrange for submission of three to five letters of recommendation. Applicants for the Associate level position should provide contact names and addresses for three to five references. All application materials must be submitted through AP Recruit at: for Assistant Professor applicants and/or for early Associate Professor applicants. Review of applications will begin on November 15, 2017. Applications will be accepted until the position is filled. Advancement through the faculty ranks at the University of California is through a series of structured, merit-based evaluations, occurring every 2-3 years, each of which includes substantial peer input. For more information about the position, please contact Dr. Jikui Song, Department of Biochemistry, University of California, Riverside (). Additional information about the Department of Biochemistry can be found at: , and for the campus, visit . The University of California is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other characteristic protected by law. UCR is a world-class research university with an exceptionally diverse undergraduate student body. Its mission is explicitly linked to providing routes to educational success for underrepresented and first-generation college students. A commitment to this mission is a preferred qualification. Education, training, experience: Basic Qualifications Ph.D. or M.D. or equivalent degree in biochemistry or a related discipline is required, as well as postdoctoral experience and a strong record of original research accomplishments. Preferred Qualifications A demonstrated potential to develop a successful independent research program in any area of physical biochemistry/Cryo-electron microscopy, with an emphasis in understanding processes of fundamental biological or biomedical relevance. Preference will be given to applicants whose research interests complement those of existing faculty in physical biochemistry and biophysics, including faculty using X-ray crystallography, NMR and single-molecule methods to study DNA repair, epigenetics, regulation of translation and cell signaling. UCR is a world-class research university with an exceptionally diverse undergraduate student body. Its mission is explicitly linked to providing routes to educational success for underrepresented and first-generation college students. A commitment to this mission is a preferred qualification.
Oct 31, 2017
Full time
Job Description: The Department of Biochemistry at the University of California, Riverside invites applications for a new 9-month faculty position at the Assistant Professor (tenure-track) or early Associate Professor level (tenured) in the general area of physical biochemistry, with a particular emphasis in the application of Cryo-EM to investigate problems of fundamental biological and biomedical importance. The position will build on existing campus strengths in structural biology and related areas of biophysics, including faculty using X-ray crystallography, NMR and single-molecule methods to study DNA repair, epigenetics, regulation of translation and cell signaling. The successful candidate will have a record of original research accomplishments; some experience in grant/fellowship proposal preparation is desirable. S/he will be expected to develop a vigorous, independent, and internationally recognized research program that is able to attract extramural funding; s/he will also develop and teach graduate and undergraduate courses, advise and mentor graduate and undergraduate students, and engage in both campus and professional service activities. A competitive start-up package will be provided, with salary commensurate with education, training and experience. The position is available July 1, 2018. A Ph.D., M.D., or equivalent degree in biochemistry or a related field is required, as well as postdoctoral experience. Interested individuals should submit a cover letter, a full curriculum vitae, a statement of research, a statement of teaching philosophy, and a statement of contributions to diversity. In addition, applicants for the Assistant level position should arrange for submission of three to five letters of recommendation. Applicants for the Associate level position should provide contact names and addresses for three to five references. All application materials must be submitted through AP Recruit at: for Assistant Professor applicants and/or for early Associate Professor applicants. Review of applications will begin on November 15, 2017. Applications will be accepted until the position is filled. Advancement through the faculty ranks at the University of California is through a series of structured, merit-based evaluations, occurring every 2-3 years, each of which includes substantial peer input. For more information about the position, please contact Dr. Jikui Song, Department of Biochemistry, University of California, Riverside (). Additional information about the Department of Biochemistry can be found at: , and for the campus, visit . The University of California is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other characteristic protected by law. UCR is a world-class research university with an exceptionally diverse undergraduate student body. Its mission is explicitly linked to providing routes to educational success for underrepresented and first-generation college students. A commitment to this mission is a preferred qualification. Education, training, experience: Basic Qualifications Ph.D. or M.D. or equivalent degree in biochemistry or a related discipline is required, as well as postdoctoral experience and a strong record of original research accomplishments. Preferred Qualifications A demonstrated potential to develop a successful independent research program in any area of physical biochemistry/Cryo-electron microscopy, with an emphasis in understanding processes of fundamental biological or biomedical relevance. Preference will be given to applicants whose research interests complement those of existing faculty in physical biochemistry and biophysics, including faculty using X-ray crystallography, NMR and single-molecule methods to study DNA repair, epigenetics, regulation of translation and cell signaling. UCR is a world-class research university with an exceptionally diverse undergraduate student body. Its mission is explicitly linked to providing routes to educational success for underrepresented and first-generation college students. A commitment to this mission is a preferred qualification.