- WuXi AppTec (Cranbury, NJ)
- **Overview** The AD Project Manager will be responsible for managing projects within STA, WuXi's API, and Drug Product development and manufacturing division. Leads ... the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development team.… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Principal Scientist ( Associate Director ) is responsible for developing and implementing Regulatory ... development, marketing applications and post-approval life cycle maintenance phases. The Associate Principal Scientist may also support project team goals… more
- Merck (Rahway, NJ)
- **Job Description** GRACS CMC - Associate Principal Scientist, CMC , R4 - Pharm Pre-approval Reporting to the Sr Director / Director /Principal ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Bristol Myers Squibb (Summit, NJ)
- …but not limited to, continued process verification. The role collaborates across all CMC functional areas to ensure project advancement, rapid and best in ... for process risks + Able to manage time and elevate relevant issues to project lead and line management. + Detail oriented with excellent verbal and written… more
- Merck (Rahway, NJ)
- …regulatory submissions. Under the general scientific and administrative direction of the Director in Biologics Cell Culture Sciences group and working in conjunction ... role, the successful candidate will be responsible to** + Coordinate project planning, resourcing, progress reporting, troubleshooting and people management. + Serve… more