Amneal Pharma Hiring for IPQA

A leading pharmaceutical manufacturing company located at Pharmez Special Economic Zone (SEZ), Ahmedabad, is hiring an Officer – IPQA (In-Process Quality Assurance) for full-time roles. This opportunity is ideal for B.Pharm, M.Pharm, or MSc graduates with hands-on experience in GMP, shop-floor QA, batch record review, deviation handling, and CPV.

This IPQA Officer job in Ahmedabad offers exposure to regulated manufacturing environments and strong career growth within quality assurance operations.

📌 Job Overview

• Position: Officer – IPQA
• Job Location: Pharmez SEZ, Ahmedabad, Gujarat
• Job Type: Full-Time
• Industry: Pharmaceutical Manufacturing
• Experience Required: Minimum 1 year (IPQA / QA Operations)
• Last Date to Apply: 13 February 2026

🔬 Key Responsibilities (IPQA Officer)

As an IPQA Officer, you will be responsible for ensuring GMP compliance and quality oversight across manufacturing and packaging operations:

• Perform machine and area clearance during dispensing, manufacturing, and packaging.
• Carry out in-process checks, AQL, and ANSI sampling as per SOPs, BMR, and BPR.
• Sample and manage blend, finished product, reserve, stability, hold-time, and in-process samples.
• Verify raw material dispensing activities and packaging batch coding details.
• Review executed Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
• Prepare and review CPV (Continued Process Verification) trend data.
• Perform impact assessments for equipment breakdowns.
• Initiate and review change controls, deviations (planned/unplanned), and quality notifications.
• Review cleaning logs, equipment logs, calibration records, and environmental monitoring data.
• Perform calibration of IPQA instruments.
• Review and approve packaging artworks, proofs, and shade cards.
• Ensure proper labeling, storage, handling, and dispensing of printed packaging materials.
• Prepare, revise, and maintain functional SOPs.
• Archive executed quality documents as per data integrity requirements.

🎓 Qualifications & Eligibility

• Education:
  • B.Pharm / M.Pharm / MSc (Chemistry, Life Sciences or related)
• Experience:
  • Minimum 1 year experience in IPQA / QA Operations within a pharma manufacturing setup
• Key Skills:
  • GMP compliance
  • BMR/BPR review
  • Deviation & Change Control
  • CPV & Trend Analysis
  • Environmental Monitoring
  • Regulatory & GxP documentation

💼 Salary & Benefits

• Estimated Salary: ₹3.0 – ₹4.5 LPA (based on experience & industry standards)
• Exposure to regulated pharma manufacturing (SEZ environment)
• Structured QA processes & documentation systems
• Career growth in Quality Assurance & Compliance
• Professional work culture with continuous learning

📝 How to Apply

Application Link