Global Regulatory Affairs Lead (CMC and Development
watton hallGermany • New York, United States • United Kingdom
Posted January 5, 2026
Full Time
About the Company
Watton Hall is an independent search and selection firm that specializes in recruiting life‑science professionals for the pharmaceutical, biotech, CRO, and medical device sectors. The company delivers executive, permanent, and contract placements at the mid to senior level, partnering closely with HR teams, on‑site recruiters, RPOs, and line managers to source top talent. By combining deep industry expertise with a cost‑effective, high‑quality partnership model, Watton Hall provides tailored recruitment solutions—including interim staffing, relocation, and conference services—to meet the evolving needs of life‑science organizations.
Job Description
We are looking for an experienced individual in Global CMC Regulatory Affairs to join our dynamic team. The successful candidate will lead regulatory strategy and submissions for innovative biopharmaceutical products and work closely with cross-functional teams to ensure compliance with global regulatory requirements.
Requirements
- Scientific degree or any related discipline
- Strong professional working experience in global CMC regulatory strategy leading activities
- Knowledge of the interdisciplinary functions involved in CMC drug development and the application of clinical research to drug development
- Combination of strategic and operational skills
Benefits
- Competitive salary
- Remote working opportunity
- Excellent company culture
- Exposure to a dynamic and evolving Biotech company