- 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)
- …department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New ... Jersey research facility. The Associate Principal Scientist is a...+ Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.… 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
- 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)
- …in compliance with departmental and company Standard Operating Procedures, regulatory requirements, and standards. **Primary Activities** **:** + Business System ... processes, assuring they are of high quality and complaint with regulatory requirements **Skills** **Education and Minimum Requirement** **:** + BA/BS in… 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)
- …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
- Pfizer (Pearl River, NY)
- …and publications. + May contribute budget execution of protocols. **Interact with regulatory authorities, key opinion leaders, and principal investigators:** + ... clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of safety data review… more
- Pfizer (Pearl River, NY)
- …and publications. + May contribute budget execution of protocols **Interact with regulatory authorities, key opinion leaders, and principal investigators:** + ... clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of safety data review… more
- Pfizer (Pearl River, NY)
- …for the on-time and within-budget execution of protocols **Interact with regulatory authorities, key opinion leaders, and principal investigators.** + ... expertise to steer clinician medical monitors, clinician clinical scientists, clinical scientist leads, and other clinical staff members. The clinician medical… more