- 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** We are seeking a Director ( Principal Scientist ), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... our pipeline and drive our strategic priorities. The Director, Principal Scientist | Regulatory Affairs...labeling and obtain shortest time to approval by global regulatory agencies. + Reports to Associate Vice… more
- Merck (Rahway, NJ)
- **Job Description** We are seeking a Senior Director (Sr. Principal Scientist ) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset ... our strategic priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs...GRACS. **Key Functions** + Reports to Executive Director or Associate Vice President, General Medicine + Works Independently and… 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)
- …growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist to advance and commercialize the intravitreal ... to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The...As a member of the drug product team, the Associate Principal Scientist will be… more
- Merck (Rahway, NJ)
- …the growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist who is an experienced drug product ... transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist , General Medicine Publications Medical Writing, works with scientists in our company's Research Labs ... other of our Research & Development Division science. The Associate Principal Scientist is expected...Translational Medicine, Global Medical and Scientific Affairs, and Global Regulatory Affairs and Clinical Safety to identify key issues… 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)
- …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)
- …analysis and high-quality data to support decision making in clinical trials. The Associate Principal Scientist , Statistical Programmer supports the design, ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- Merck (Rahway, NJ)
- …assays that are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position should have strong technical expertise ... validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials.… 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)
- …data + Produce tables and graphics for inclusion in study reports and regulatory submissions + Ensure programmatic traceability from data source to modeling result + ... + produce SAS transport files and associated documentation for regulatory submissions + Represent statistical programming on process improvement activities… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …every treatment we pioneer. Join us and make a difference. Position Summary The Principal Process Engineer/ Scientist acts as a technology transfer lead in the ... cGMPs, BMS procedures, and that processes are defined consistent with regulatory filings. This position must comply with all Security guidelines, Environmental… 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