
Scientist, Global Regulatory Affairs CMC
- København
- Permanent
- Fuldtid
- Review CMC documents for submissions as relevant
- Review Change Requests
- Prepare and update Master Submission index for module 3/ASMF's/DMF's
- Prepare and update Quality Overall Summaries (for mature products)
- Prepare CMC related administrative documents for submissions as relevant
- Prepare responses to CMC related authority questions
- Comment on guidelines and pharmacopoeia monographs
- BA/BS degree in a scientific/engineering discipline
- 1-3+ years of experience in the pharmaceutical industry
- Experience with CTD format and content regulatory filings
- Effective communication and interpersonal skills to effectively collaborate with cross-functional teams and external stakeholders.
- Informal approach to stakeholders and colleagues