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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Solid 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.

📌 IPQA for Pharmaceutical Company (Amreli)
🏢 Pramukh Staffing
📍 Amreli