5 years
0 Lacs
Posted:11 hours ago|
Platform:
On-site
Full Time
✅ Manage post-approval changes (Annual Reports, CBE-30)
✅ Review technical documents: analytical validation, specifications, stability data, batch manufacturing records
✅ Ensure compliance across all regulatory guidelines
2–4 years in Regulatory Affairs within the pharmaceutical industry, preferably with exposure to regulated markets.
Softgel Healthcare Private Limited
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