IPQA Executive
Job Description:
Key Responsibilities:
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Perform in-process checks during manufacturing and packaging (weight variation, hardness, friability, disintegration, pH, viscosity, leak test, etc.).
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Ensure batch manufacturing records (BMR/BPR) are correctly filled and compliant.
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Monitor line clearance, environmental conditions, and GMP practices on shop floor.
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Review and verify critical process parameters (CPP) and ensure adherence to SOPs.
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Check and approve equipment cleanliness, status labels, and area clearance.
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Conduct sampling for IPC tests and coordinate with QC for timely results.
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Report deviations, OOS, OOT, or non-compliance during process activities.
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Ensure online documentation, traceability, and batch integrity.
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Monitor packing line activities like coding, labeling, and correct reconciliation of materials.
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Support investigations, CAPA implementation, and continuous improvement.
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Ensure compliance with cGMP, GDP, and regulatory guidelines during all operations.
Desired Profile / Criteria / Skills :
Required Skills & Qualifications:
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B.Pharm / M.Pharm / B.Sc / M.Sc.
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1–5 years experience in IPQA (Formulation).
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Strong knowledge of manufacturing processes (tablets, capsules, liquids, injectables – as applicable).
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Good understanding of SOPs, BMR/BPR, QA documentation, and compliance standards.
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Ability to handle shop-floor monitoring and real-time decision-making.
Company Profile
Our client followa standards of WHO - CGMP
Our Mission
“To become a valued Pharmaceutical partner to the World Pharma fraternity by continuously researching, developing and manufacturing a wide range of pharmaceutical products that complies with the global regulatory standards.”
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.