Key Responsibilities:
- Review Analytical and Batch Manufacturing Records (BMR) for data integrity and compliance.
- Manage Quality Management System (QMS) documents, including Deviations, CAPA (Corrective and Preventive Actions), and Change Controls.
- Oversee in-process quality control (IPQC) and line clearance during chemical/API manufacturing.
- Ensure all laboratory and production operations meet cGMP/GLP and FDA/ICH guidelines.
Required Skills: BSc/MSc in Chemistry or B.Pharm/M.Tech, extensive knowledge of regulatory audits, and chemical testing protocols
Pay: ₹300,000.00 - ₹500,000.00 per year
Work Location: In person
