- Perform IPQA activities during manufacturing and packaging operations.
- Ensure compliance with GMP, SOPs, BMR/BPR and approved procedures.
- Review and maintain Batch Manufacturing & Packaging Records and other QA documents.
- Handle deviations, OOS/OOT, CAPA and change controls.
- Conduct line clearance, in-process checks and area inspections.
- Ensure proper documentation and data integrity as per ALCOA+ principles.
- Coordinate with Production, QC and other departments for batch release documentation.
- Support internal audits, regulatory inspections and quality system activities.
Qualification
B.Pharm / M.Pharm / M.Sc. / B.Sc. or equivalent.
Required Skills
- 3–5 years of experience in Pharmaceutical QA/IPQA & Documentation.
- Valuable knowledge of cGMP, GDP, SOPs and documentation practices.
- Strong attention to detail and good communication skills.
Pay: ₹12,000.00 - ₹15,000.00 per month
Ability to commute/relocate:
- Derabassi, Punjab: Reliably commute or planning to relocate before starting work (Preferred)
Experience:
- Microbiology: 1 year (Required)
Work Location: In person
📌 QA Analyst (India)
🏢 UV LIFECARE
📍 India
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