Executive - Quality Assurance, Pharma

• B. Pharm / M. Pharm from a reputed university

• 3 to 6 years of similar experience in a regulatory-approved OSD manufacturing large unit.

• Lead deviation and market complaint investigations, with timely CAPA execution
• Ensure effective implementation and tracking of CAPAs from deviations & complaints
• Review Batch Manufacturing & Packing Records, APQR, and SOPs
• Manage Change Controls, Validations/Qualifications, and QMS documentation
• Conduct regulatory gap assessments and support compliance plan execution
• Coordinate GMP training, documentation control, and audit readiness

• 3 to 6 years of QA experience in pharmaceutical manufacturing (formulations)
• Strong understanding of cGMP, investigation tools, and regulatory expectations (USFDA, MHRA)
• Skilled in QMS systems.
• Excellent documentation, analytical, and coordination skills

Zentiva