- 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 22-Aug-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)
- …to develop the new veterinary products that will make animals healthier. The Associate Principal Scientist , Animal Health Clinical Research position designs, ... Clinical Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study… 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)
- **Job Description** **Position Description:** **Device Development Associate Principal Scientist - Development Strategy, Design Controls and Risk ... to ensure they are developed and manufactured in accordance with regulatory , company, and customer requirements. ** Principal Responsibilities** + Lead/contribute… 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
- 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)
- …Cell Based Sciences team in Rahway, NJ is seeking a motivated scientist with technical expertise in **Biologics Potency** assays in drug **Development** . ... context of broader process and product development. + Working knowledge of regulatory guidance and quality standards, with experience authoring and reviewing … 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 ... projects in Late Development Statistics. + Interacts with Clinical, Regulatory , Statistical Programming, Data Management, and other company Research Laboratories… 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