Specialist Regulatory Affairs-CMC (m/f/d)
MSD(18 days ago)
About this role
This role involves managing the quality part (CMC) of registration dossiers for animal medicines, including documentation, compliance, and regulatory communication, within a global pharmaceutical environment. It emphasizes collaboration with teams and external agencies to ensure timely and accurate regulatory submissions.
Required Skills
- regulatory Affairs
- Compliance
- Documentation
- System Management
- Pharmaceutical Industry
- Regulatory Communications
- Quality Standards
- Audits
- eCTD
- Lab Management
About MSD
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