:

Key Responsibilities:

- Perform in-process checks during manufacturing and packaging (weight variation, hardness, friability, disintegration, pH, viscosity, leak test, etc.).

- Ensure batch manufacturing records (BMR/BPR) are correctly filled and compliant.

- Monitor line clearance, environmental conditions, and GMP practices on shop floor.

- Review and verify critical process parameters (CPP) and ensure adherence to SOPs.

- Check and approve equipment cleanliness, status labels, and area clearance.

- Conduct sampling for IPC tests and coordinate with QC for timely results.

- Report deviations, OOS, OOT, or non-compliance during process activities.

- Ensure online documentation, traceability, and batch integrity.

- Monitor packing line activities like coding, labeling, and correct reconciliation of materials.





- Support investigations, CAPA implementation, and continuous improvement.

- Ensure compliance with cGMP, GDP, and regulatory guidelines during all operations.

Desired Profile / Criteria / Skills :

Required Skills & Qualifications:

- B.Pharm / M.Pharm / B.Sc / M.Sc.

- 1–5 years experience in IPQA (Formulation).

- Strong knowledge of manufacturing processes (tablets, capsules, liquids, injectables – as applicable).

- Positive understanding of SOPs, BMR/BPR, QA documentation, and compliance standards.

- Ability to handle shop-floor monitoring and real-time decision-making.

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