Associate Director, Global Regulatory Affairs CMC
GenmabCopenhagen, Capital Region of Denmark, Denmark
Posted March 3, 2026
Full Time
About the Company
Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics.
Job Description
Genmab is seeking an Associate Director to join the Regulatory Affairs CMC team to provide strategic and operational regulatory CMC expertise across the global lifecycle of commercialized products.
Requirements
- Master of Science in pharmacy, engineering or equivalent
- Minimum 5-10 years of industry experience within Regulatory Affairs CMC
- A track record in moving therapeutic products through various stages of development
- Experience with lifecycle management
- Proficient communication in English (verbal and written)
- Excellent collaboration and communication skills
- Ability to work independently and drive projects to successful outcomes
- Quality mindset and ability to prioritize work in a fast-paced environment
- Result-oriented and committed to contributing to the overall success of Genmab
Benefits
- Generous Paid Time Off
- 401k Matching
- Tuition Reimbursement