23 Aug
|
Ami Lifesciences
|
India
23 Aug
Ami Lifesciences
India
Role & responsibilities
Preparation, review, and submission of regulatory dossiers (DMF, CEP, etc.)
Handling regulatory queries and deficiency responses
Compilation and review of technical documents in line with global requirements
Coordination with cross-functional teams (R&D;, QA, QC, Production)
Ensuring compliance with international regulatory guidelines
Preferred candidate profile
•M.Sc. Organic / Analytical Chemistry / M.Pharma
2 to 10 years of experience in API Industry
📌 Regulatory Affairs Api Vadodara (India)
🏢 Ami Lifesciences
📍 India