We are looking for an experienced Quality Assurance skilled with 10–12+ years of experience in pharmaceutical API / bulk drug manufacturing.
Key Responsibilities:
Ensure compliance with cGMP, pharmaceutical quality systems, and regulatory requirements.
Review and approve SOPs, BMRs, specifications, protocols, and quality documents.
Handle Deviations, CAPA, Change Controls, OOS/OOT investigations, and Risk Assessments.
Support internal audits, vendor audits, customer audits, and regulatory inspections.
Review validation and qualification documents.
Coordinate with Production, QC, Warehouse, and other departments to ensure quality compliance.
Conduct GMP training and support continuous quality improvement initiatives.
Qualification: B.Pharm, M.Pharm, B.Sc./M.Sc. Chemistry or equivalent. Location: Kadechur, Karnataka.