The Officer - IPQA will support in-process quality assurance activities for manufacturing and packaging, shop floor compliance, line clearance, documentation review, deviation reporting, and GMP monitoring at Ipca Laboratories Limited, Vapi. This requires B.Pharm qualification with 2–4 years of IPQA experience.
Roles & Responsibilities
- Perform IPQA checks during manufacturing and packaging activities.
- Verify line clearance, area readiness, material status, equipment cleanliness, and process compliance.
- Review batch manufacturing records, batch packing records, logbooks, and shop floor documents.
- Monitor critical process parameters and ensure activities are performed as per SOPs.
- Check in-process samples, packing details, labels, coding, and reconciliation records.
- Report deviations, non-compliance, documentation gaps, or quality concerns promptly.
- Coordinate with production, packing, QA, QC, warehouse, and engineering teams.
- Support GMP rounds, audit readiness, and quality system compliance.
- Maintain proper documentation as per GDP and data integrity requirements.
- Ensure quality-focused and compliant manufacturing and packaging operations.