- 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 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
- Merck & Co. (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions.-Under the general scientific and administrative direction of the ... next generation process development and characterization, process validation, and regulatory submission authoringIn this role, the successful candidate will be… more
- Merck & Co., Inc. (North Wales, PA)
- …and unplanned statistical analyses. Prepare compliant programming code for regulatory submissions including analysis/modeling datasets, tables, listings, figures and ... associated documentation. Ensure programmatic traceability from data source to analysis/modeling result. Maintain and manage a project plan including resource forecasting. Support the development of programming standards to enable efficient and high-quality… more
- TriCore Reference Laboratories (Albuquerque, NM)
- …2. Notes abnormal patient results and informs supervisor, pathologist, or principal investigator as appropriate. 3. Operates laboratory equipment, interfaces and ... recommends appropriate solutions using defined guidelines. 6. Actively participates in regulatory inspections. 7. Takes inventory as needed or appropriate. Orders… 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
- 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
- L'Oreal USA (Clark, NJ)
- …(https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 206467 Associate Principal Clinical Research ... Jersey Clark, NJ Research & Innovation Full - Time 27-May-2025 Position Title: Associate Principal Clinical Research Scientist , Open Clinical Innovation… 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
- 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** 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
- Bristol Myers Squibb (Princeton, NJ)
- …track record of high-quality scientific publications in relevant fields For the Sr. Principal Scientist position, the starting compensation for this job is a ... oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external… 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
- Bristol Myers Squibb (Devens, MA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Principal Scientist is a subject matter expert, project owner and ... investigator supporting commercial biologics manufacturing at Bristol-Myers Squibb Devens. The Principal Scientist will oversee and deliver complex technical… more
- Merck (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions. Under the general scientific and administrative direction of ... next generation process development and characterization, process validation, and regulatory submission authoring **In this role, the successful candidate will… 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
