- Organon & Co. (Jersey City, NJ)
- …the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate Director) is responsible for ... and will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team… more
- Merck (Rahway, NJ)
- **Job Description** **Brief Description of Position** The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine ... Affairs and Clinical Safety **Job Level/ Grade** 400 **Reports to** Global Regulatory Liaison, Executive Director or Associate Vice President, Section Head… more
- L'Oreal USA (Clark, NJ)
- …(https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 187395 Associate Principal Scientist , ... Research & Innovation Full - Time 01-Sep-2024 Position Title: Associate Principal Scientist , Cosmetics Product...New Jersey (Hybrid) Department : Product Safety, SRCM (Safety, Regulatory , Claims, & Microbiology) For more than one hundred… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description:** ** Associate Principal Scientist , Statistical Programming** The Associate Principal Scientist , ... 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 (Rahway, NJ)
- …knowledge in both analytical experimental design and biotherapeutic pipeline programs. Finally, this Associate Principal Scientist will be a partner in ... Mass Spectrometry -group in Rahway, NJ is seeking a motivated scientist with technical expertise in mass spectrometry-based protein characterization. This position… more
- Merck (Rahway, NJ)
- …drug products. Our team is looking for a candidate for the position of Associate Principal Scientist (R4) supporting the Biologics formulation team within ... packaging, compatibility characterization for processing and administration, and supporting regulatory filings. + Build deep fundamental knowledge around the drug… more
- Merck (Rahway, NJ)
- …& Product Modeling Team in our Company Manufacturing Division seeks an experienced Associate Principal Scientist who will develop and utilize advanced ... and cGMP environments is highly desired. Familiarity or experience with regulatory filings (BLAs, NDAs) and CMC processes preferred. + Experience with… more
- Bristol Myers Squibb (Summit, NJ)
- …difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of the late stage TM ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… more
- Merck (Rahway, NJ)
- …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 (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... Data Repositories. + United States and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- Merck (Rahway, NJ)
- …interpreting LC-MS/MS data under the supervision of study director/supervisor/ Principal investigator/line manager. + Developing, optimizing and implementing ... accurate and compliant with current GLP and departmental guidelines under the Principal Investigator's oversight. + Preparing reports for drug discovery and non-GLP… more
- Merck (Rahway, NJ)
- **Job Description** The **Senior Clinical Director (Sr. Principal Scientist )** has primary responsibility for the strategic planning and directing clinical ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Clinical Director May… more