Location: Thane (Work From Office | 5 Days a Week)
Qualification: B. Pharm / M. Pharm / M.Sc
Key Responsibilities:
End-to-end post-approval life cycle management for regulated markets
Handling variation submissions and renewal submissions for EU and UK
Expertise in Module 1 and Module 3 documentation
Coordination with internal teams and regulatory agencies to ensure compliance
Updating dossiers and ensuring timely submissions.
We are looking for experienced Regulatory Affairs professionals with strong expertise in post-approval life cycle management.
Interested candidates with relevant experience may share their profiles at asharma@crescentpharma.com
No comments:
Post a Comment