A leading pharmaceutical manufacturing company located at Pharmez Special Economic Zone (SEZ), Ahmedabad, is hiring an Officer โ 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.
๐ Job Overview
- Position: Officer โ 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
๐ฌ 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.
๐ 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
๐ผ Salary & Benefits
- Estimated Salary: โน3.0 โ โน4.5 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