- Merck & Co. (Rahway, NJ)
- Job DescriptionAs the Director / Principal Scientist in Devices and Drug-Device Combinations CMC (Chemistry, Manufacturing & Controls), you will report to the ... Director of Device Regulatory Affairs for Autoinjector Development Programs. You will spearhead regulatory activities for Devices and Drug-Device Combinations… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionWe have an exciting opportunity for a- Principal Scientist ( Director ) in Translational Medicine. Translational Medicine at our Research ... Clinical Research while developing and expanding your career.Primary responsibilities for the Principal Scientist include the following:Key member of an early… more
- Merck & Co. (Rahway, NJ)
- …talented and dedicated colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist ) has primary responsibility for ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May… more
- Merck & Co. (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career.--The Director ( Principal Scientist ) has primary responsibility for the ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be… more
- Merck & Co. (Rahway, NJ)
- …products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional ... and influence clinical and commercial combination product development and launches. Principal ResponsibilitiesLead and set direction for the device development… more
- Merck & Co. (Rahway, NJ)
- …sites, manufacturing investigations, process validation, and authoring of regulatory submissions. -Under the general scientific and administrative direction ... of Director in the CCFS group and working in conjunction...next generation process development and characterization, process validation, and regulatory submission authoring. In this role, the successful candidate… more
- Merck & Co. (Rahway, NJ)
- …and dedicated colleagues while developing and expanding your career. - The Senior Director (Senior Principal Scientist ) has primary responsibility for the ... analysis, regulatory reporting, and publication. - Specifically, the Senior Director may be responsible for Evaluating pre-clinical and translational work for… more
- Merck (Columbus, OH)
- **Job Description** As the Director / Principal Scientist in Devices and Drug-Device Combinations CMC (Chemistry, Manufacturing & Controls), you will report to ... the Director of Device Regulatory Affairs for Autoinjector Development Programs. You will spearhead regulatory activities for Devices and Drug-Device… more
- AbbVie (Irvine, CA)
- …Aesthetics on LinkedIn. The Neurotoxin Research Group at AbbVie seeks an accomplished scientist and leader. The Director /Senior Principal Research ... productive, collaborative, and inclusive laboratory environment in compliance with regulatory and company expectations. Experience managing projects from early-stage… more
- Merck (West Point, PA)
- …ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead ... and influence clinical and commercial combination product development and launches. ** Principal Responsibilities** + Lead and set direction for the device… more
- Abbott (St. Paul, MN)
- …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Principal Clinical Scientist ** **Working at Abbott** At Abbott, you can do ... device and management solutions for treating structural heart disease. The Principal Clinical Scientist will provide scientific expertise throughout the… more
- Merck (Boston, MA)
- **Job Description** We have an exciting opportunity for a ** Principal Scientist ( Director ) in Translational Medicine** . Translational Medicine at our ... Clinical Research while developing and expanding your career. **Primary responsibilities for the Principal Scientist include the following:** + Key member of an… more
- Merck (North Wales, PA)
- …talented and dedicated colleagues while developing and expanding your career. The Senior Director (Senior Principal Scientist ) has primary responsibility for ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director … more
- Merck (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career. The Director ( Principal Scientist ) has primary responsibility for the ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may… more
- UTMB Health (Galveston, TX)
- …utilize the US FDA GLP regulations as a reference standard. The Regulatory Scientist II may also function as a Principal Investigator for extramurally funded ... Regulatory Scientist I / II -...Principal Investigator. Indirect: May assist the ORNcS Scientific Director with institutional budget planning. **DECISION-MAKING RESPONSIBILITY** Project management… more
- Merck (West Point, PA)
- …we collaborate to discover the next medical breakthrough. We are seeking a Principal Scientist to join our Vaccine Analytical Research and Development team ... West Point, PA. In this role, an individual will work closely with the group Director to define group strategy and lead a team of scientists in solving complex… more
- Abbott (Santa Clara, CA)
- …Mechanical Engineers, Product Development Engineers, and Manufacturing Engineers. This scientist will provide technical leadership and guidance towards the ... in design, development, manufacturing, and/or use of Abbott products, support regulatory filings related to materials science, and design and execute research… more
- Hackensack Meridian Health (Edison, NJ)
- …to transform healthcare and serve as a leader of positive change. The ** Director , Member Scientist , Clinical Research** is responsible for initiating, leading ... research in brain injury. **Responsibilities** A day in the life of a ** Director , Member Scientist , Clinical Research** at Hackensack Meridian _Health_ includes:… more
- Merck (Rahway, NJ)
- …sites, manufacturing investigations, process validation, and authoring of regulatory submissions. Under the general scientific and administrative direction ... of Director in the CCFS group and working in conjunction...next generation process development and characterization, process validation, and regulatory submission authoring. **In this role, the successful candidate… more
- Sutter Health (San Francisco, CA)
- …as periodically summarizing QC and PT results in reports or graphs for Medical Director review. Also performs a variety of Quality Assurance (QA) duties such as ... in maintaining accreditation readiness; participates in accreditation surveys and regulatory agency inspections. Advises on, and provides guidance for, technical… more
