
Regulatory CMC Consultant
- Surrey
- Contract
- Full-time
- Lead regulatory strategy and CMC submission preparation for solid, liquid, and parenteral formulations across Europe, the UK, and Switzerland.
- Review and update outdated CMC documentation to meet current regulatory expectations.
- Act as a Subject Matter Expert for CMC variations.
- Balance strategic regulatory planning with submission execution.
- Strong knowledge of EU regulatory procedures, including MRP, DCP, and NP.
- In-depth understanding of CMC regulatory requirements and ICH guidelines.
- Hands-on experience preparing CMC variations and navigating European regulatory frameworks.
- Ability to work independently and provide guidance on legacy dossier lifecycle management.
- Expertise in developing regulatory strategies and coordinating cross-functional teams.
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