We are looking for a Quality Assurance professional to ensure product quality, regulatory compliance, and adherence to cGMP standards throughout the manufacturing process of APIs and bulk drugs.
Key Responsibilities:
Monitor and review manufacturing and testing processes to ensure compliance with GMP, GLP, and SOPs.
Prepare and review quality documents, protocols, deviations, and change controls.
Conduct in-process checks, line clearance, and batch record reviews.
Coordinate with QC, Production, and Regulatory teams for smooth operations and audits.
Ensure timely compliance with internal, external, and regulatory audits.
Job Requirements:
B.Sc / M.Sc / B.Pharm / M.Pharm in Chemistry or related field.
Fresher or 1–3 years of QA experience in Pharma preferred.
Strong knowledge of GMP, GLP, and regulatory guidelines.
Good documentation, analytical, and communication skills.