A
Ami Lifesciences
Regulatory Affairs | API
Skills
Testing & QARCompliance
2 months ago
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Important information
Contract type:
Permanent
Location:
Vadodara, Gujarat, India
Work mode:
Onsite
Published on:
19 August 2026
What they need
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
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