IPQA Officer

Roles & Responsibilities
• Perform in-process quality assurance activities on the manufacturing shop floor
• Monitor manufacturing and packing operations to ensure GMP compliance
• Review and approve Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
• Handle deviations, change controls, and corrective & preventive actions (CAPA)
• Support process validation, cleaning validation, and continued process verification (CPV)
• Conduct line clearance and in-process checks
• Ensure compliance with SOPs, regulatory guidelines, and quality standards
• Participate in internal audits, regulatory inspections, and customer audits
• Coordinate with Production, QC, and Engineering teams for quality-related activities

Qualification
• B.Pharm / M.Pharm / M.Sc (Chemistry / Life Sciences or related discipline)

Experience
• 1–4 years of relevant experience in IPQA or shop-floor QA in pharmaceutical manufacturing

Skills
• Strong knowledge of GMP and IPQA processes
• Experience in batch record review and deviation handling
• Familiarity with CPV, validation activities, and quality documentation
• Good understanding of shop-floor operations
• Strong attention to detail and documentation skills
• Ability to work effectively in cross-functional teams

About the Organization
The organization is a leading pharmaceutical manufacturing company located at Pharmez Special Economic Zone (SEZ), Ahmedabad, operating in regulated markets with a strong focus on quality, compliance, and continuous improvement, offering excellent career growth in quality assurance operations.