package ready for submission.
Responsibilities Contribute to the phase appropriate development strategy for the Biologics portfolio.
Write and edit CMC sections of Regulatory documents that are submitted to Regulatory Agencies worldwide. Experience with authoring Module 3
Full-time- ID: #54721200
- State: Delaware Wilmington 19801 Wilmington USA
- City: Wilmington
- Salary: USD TBD TBD
- Showed: 2025-10-26
- Deadline: 2025-12-22
- Category: Writing/editing