- Cytokinetics (South San Francisco, CA)
- …and company standards. Collaborate with cross-functional teams (eg, Quality Assurance, Regulatory Affairs , Global Supply Chain) to gather necessary information ... regulatory requirements. Key Responsibilities: Organize, maintain, and archive CMC , Technical Operations, and Manufacturing documentation. Ensure all CMC ,… more
- Kelly Services (Bridgeton, MO)
- **Kelly Science has an Immediate opening for a CMC Regulatory Sciences Specialist for our growing client near St. Louis, MO** Full-time Direct Hire Hybrid ... Compliance & Submissions** + Prepare, review, and submit high-quality postapproval CMC regulatory submissions and related correspondence to the FDA/CVM. +… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …position to act as a team member in the product manager area of Regulatory Affairs (Biopharma) supporting global submissions for various areas of the business. ... to support business needs in a very timely and accurate manner. **_Sr Reg Affairs Specialist I_** **Primary responsibilities for role:** + Act as Regulatory… more
- Kelly Services (Bridgewater, NJ)
- ** Regulatory Affairs Specialist ** Kelly Science and Clinical is seeking a ** Regulatory Affairs Specialist ** **for** our client a leading medical ... **Responsibilities** + Provide support for the execution of the pharmaceutical regulatory strategy and submissions for assigned products: Provide support for… more
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