- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionGRACS CMC - Associate Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/ Principal Scientist /Sr ... 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 ... 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)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Merck & Co. (Boston, MA)
- …Bioanalytics (PDMB) in West Point, PA is seeking a highly motivated Associated Principal Scientist with wide knowledge of pharmacokinetic (PK) and toxicokinetic ... exploratory and definitive/Good Laboratory Practice (GLP)], serving as a contributing scientist / principal investigator on toxicity studies, and executing PK/TK… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Associate Principal Scientist ( Associate Director) is responsible for developing and implementing Regulatory ... with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead...projects and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
- Organon & Co. (Jersey City, NJ)
- …project teams and alliance partners to develop and implement world-wide regulatory strategies for assigned biosimilar projects, with a specific focus on ... Regulatory CMC (Chemistry, Manufacturing, and Controls) requirements. This role...development due diligence activities. **Responsibilities** + Provide global strategic regulatory CMC overview for respective products and portfolio. +… more
- Merck (Upper Gwynedd, PA)
- **Job Description** GRACS CMC - Associate Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/ Principal Scientist ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Astrix Technology (North Wales, PA)
- ** Associate Principal Scientist (Epidemiology)** Clinical North Wales, PA, US Pay Rate Low: 58.67 | Pay Rate High: 71.43 + Added - 14/04/2025 Apply for Job ... and innovative animal-health products, is in search of an Associate Principal Scientist to join...selection of an appropriate endpoint measure to satisfy both regulatory and reimbursement needs + Coordinate COA/PRO related sections… more
- Charles River Laboratories (Ashland, OH)
- …Ensure scientific Integrity of studies, with minimal oversight. * Function as a Principal Investigator, Individual Scientist , and/or Project Scientist as ... a career that you can feel passionate about. **Job Summary** Serve as a scientist in the conduct of assigned nonclinical research studies of basic complexity, to… more
- Merck (South San Francisco, CA)
- …Bioanalytics (PDMB) in West Point, PA is seeking a highly motivated Associated Principal Scientist with wide knowledge of pharmacokinetic (PK) and toxicokinetic ... exploratory and definitive/Good Laboratory Practice (GLP)], serving as a contributing scientist / principal investigator on toxicity studies, and executing PK/TK… 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 ... teams to foster collaboration and innovation. + Document Excellence: Author regulatory and technical documentation, ensuring all processes align with our company's… more
- Merck (Rahway, NJ)
- …Description** **Role Summary** + Under the guidance of a senior leader, an Associate Principal Scientist / Associate Director, has primary responsibility ... barriers to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs + In… more
- Merck (West Point, PA)
- **Job Description** We are seeking an innovative and collaborative senior scientist to join our immunotoxicology team at the West Point, PA site. As part of the ... consortia and symposia. Stay updated on the latest scientific research, regulatory guidance, and industry trends to guide informed decisions, drive innovation,… more
- Merck (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… 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
- Walmart (Bentonville, AR)
- …service operations and technology solutions for Finance, People, and the Associate Digital Experience. **About People.AI Team** The People.AI team is responsible ... intelligent experience within a chatbot or business application to enhance associate experience and productivity. You will design and build an intelligent… more
- Charles River Laboratories (Mattawan, MI)
- …and education are added correctly. **Job Summary** We are seeking an **Senior Associate Scientist ** for our **Bioanalytical Team** site located in **Mattawan, ... MI** . The following are responsibilities related to the **Senior Associate Scientist ** : An Senior Associate Scientist in Laboratory Sciences is… more
