Role & responsibilities
- API Production, Bulk Drug
- Ensure compliance with regulatory standards for quality and efficiency.
- Batch start-up activity, monitoring
- Calibration of balance
- Review technical documents like batch records, SOPs, BMR, validation protocols, etc.
- Knowledge and exposure of cGMP is must.
Preferred candidate profile
- M.Sc. in Organic Chemistry / B.Tech Chemical Engineering.
- Fresher to 1 years of experience in Production within the API industry.
- Solid understanding of GMP, documentation review, troubleshooting, and collaboration with cross-functional teams.
📌 Walk-in || Production Trainee To Officer (Ankleshwar)
🏢 Ami Lifesciences
📍 Ankleshwar
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.