- Bristol Myers Squibb (New Brunswick, NJ)
- …an author/reviewer. + Principal Scientist incumbent is experienced in building the CMC dossier for regulatory submissions within the development section ... **Position Summary** Bristol Myers Squibb is seeking a Senior Scientist or Principal Scientist to join the...assessment approaches, and cGMP principles. + Basic knowledge of regulatory requirements for the CMC dossier… more
- Bristol Myers Squibb (Summit, NJ)
- …of drug product formulation and process development principles. + Experienced in building the CMC dossier for regulatory submissions as an author/reviewer. + ... related CMC strategy development. **Key Responsibilities** The Senior Principal Scientist will collaborate across BMS sites with Analytical, Drug Product, Drug… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and external documentation. + Authors technical documents such as protocols, reports, regulatory dossier , etc for internal and external audience. + Effectively ... Gilead and help create possible, together. **Job Description** The **Research Scientist , Biologics Pre-Pivotal Formulation and Process Development** role is part of… more
Locations:
New Jersey,
California