- Merck & Co. (Upper Gwynedd, PA)
- … Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director / Principal Scientist /Sr Principal Scientist in ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls(Associate Director Equivalent) Our company's Device ... to ensure they are developed and manufactured in accordance with regulatory , company, and customer requirements.- - Principal ResponsibilitiesLead/contribute to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist /Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a ... cross-functional teams to foster collaboration and innovation.Document Excellence: Author regulatory and technical documentation, ensuring all processes align with… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist /Associate Director , has primary responsibility for ... reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programsIn collaboration… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryThe Principal Scientist / Director , Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which ... reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs.In… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director ( Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new or ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be… more
- Merck & Co. (Rahway, NJ)
- …of our Company's Research & Development Division is seeking applicants for a Principal Scientist position available at its Rahway, New Jersey research facility. ... The Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of… more
- Merck & Co. (Rahway, NJ)
- …teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing ... technology and applying rigorous scientific and ethical standards.The Senior Director has primary responsibility for the planning and directing clinical… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Principal Scientist ( Director ) Regulatory CMC is responsible for Regulatory Chemistry Manufacturing & ... management for the assigned portfolio of small molecule or biologic products. The Principal Scientist may also support project team goals and organizational… more
- Merck (Upper Gwynedd, PA)
- … Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director / Principal Scientist /Sr Principal Scientist in ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Organon & Co. (Plymouth Meeting, PA)
- …**The Position** The Associate Principal Scientist (Associate Director ) is responsible for developing and implementing Regulatory Chemistry, ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC… more
- Merck (Rahway, NJ)
- **Job Description** **Device Development Associate Principal Scientist - Development Strategy, Design Controls** **(Associate Director Equivalent)** _Our ... to ensure they are developed and manufactured in accordance with regulatory , company, and customer requirements. ** Principal Responsibilities** + Lead/contribute… more
- Merck (Rahway, NJ)
- **Job Description** Join Our Team as an Associate Principal Scientist /Associate Director in Biologics Drug Substance Commercialization! Are you ready to make ... teams to foster collaboration and innovation. + Document Excellence: Author regulatory and technical documentation, ensuring all processes align with our company's… more
- AbbVie (North Chicago, IL)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Senior Principal Research Scientist / Director of Drug Metabolism and ... of absorption, distribution, metabolism, excretion (ADME), and pharmacokinetics. + Ensure regulatory compliance for all studies and reports, providing oversight of… more
- Merck (Rahway, NJ)
- …Summary** + Under the guidance of a senior leader, an Associate Principal Scientist /Associate Director , has primary responsibility for planning/managing ... barriers to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs + In… more
- Merck (North Wales, PA)
- **Job Description** **Role Summary** + The Principal Scientist / Director , Value & Implementation (V&I) Outcomes Research, position resides in the V&I ... to reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs. + In… more
- Catalent Pharma Solutions (Baltimore, MD)
- …on Quality by Design principles and regulatory compliance. The Principal Scientist will report to the Senior Director of Analytical Development and is ... ** Principal Scientist , Analytical Development** **Summary:** Catalent...Scientist - Analytical Development will report to the Senior Director , Analytical Development. **Catalent is committed to a Patient… more
- Merck (West Point, PA)
- …to foster collaboration and innovation. + **Document Excellence** : Author regulatory and technical documentation, ensuring all processes align with our company ... Familiarity with late-stage process development, process characterization, process validation regulatory submissions, and working with external contract organizations. +… more
- Takeda Pharmaceuticals (Boston, MA)
- …life-changing therapies to patients worldwide. Join Takeda as a **Senior** ** Principal Pharmacovigilance Scientist ** where you will provide pharmacovigilance ... will contribute:** + Technically fully competent to perform all usual Principal Pharmacovigilance Scientist /Senior Pharmacovigilance Scientist workload,… more
- Merck (Rahway, NJ)
- **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be… more
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