In-Process Quality Assurance (IPQA) is a specialized function within pharmaceutical and biotechnology manufacturing dedicated to real-time shop-floor oversight and defect prevention.

Core Roles and Responsibilities

- Line Clearance: Inspect and verify that manufacturing or packaging lines are completely clean, dry, and free of residues, labels, or materials from previous batches before starting a recent operation.
- Real-Time Shop-Floor Monitoring: Oversee daily production lines to guarantee adherence to Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and internal quality policies.
- In-Process Checks (IPCs): Conduct or supervise testing during granulation, compression, coating, filling, and packaging—checking parameters such as tablet weight variation, hardness, thickness, disintegration, friability, pH, and viscosity.
- Batch Record Review: Audit Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) in real time to verify that calculations, entries,



and documentation follow strict data integrity guidelines.
- Environmental & Facility Monitoring: Track cleanroom conditions including ambient temperature, relative humidity, and differential air pressure.
- Sampling Activities: Collect official in-process samples, validation samples, and environmental monitoring samples according to approved protocols.
- Deviation & Change Control: Identify, document, and report process deviations or non-conformances, and assist with root-cause investigations and Corrective and Preventive Actions (CAPA).
- Data Integrity & Compliance: Enforce ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, Available) to prevent regulatory warnings or batch recalls.

Pay: From ₹15,000.00 per month

Work Location: In person

📌 IPQA: In-Process Quality Assurance (Dehradun)
🏢 Nutrigenica
📍 Dehradun