IPQA - Officer

PeopleStrong; Solan; On-site; INR 600,000 - 900,000; Full time

Job summary

PeopleStrong in Solan, Himachal Pradesh is seeking IPQA personnel to oversee line clearance, records monitoring, in-process activities, sampling, and process validation. The role involves strict adherence to SOPs and BMR/BPR documentation, with responsibility for calibration records and equipment checks.

The candidate will ensure proper documentation and quality control across packaging and manufacturing stages in a GMP environment.

Responsibilities

• Line clearance for Dispensing, Granulation, Blending, Compression, Capsule, Coating and Packing as per SOPs and batch records.
• Monitor and verify records across days store, Change part room, Quarantine area and Accessory room.
• Perform in-process activities per SOPs, BMR and BPR in Compression, Capsule and Packing.
• Sampling at stages like Blending, Compression, Coating, Capsule and Packing as per SOPs, BMR and sampling plan.
• Monitor validation batches at different stages and collect samples per protocol.
• Maintain IPQA documents and calibration records (semi-finish, validation, rinse water, control and finish sample registers) and calibrate equipment.

Job description

• Line Clearance:–To give the line clearance for the different activity in their concern area like Dispensing, Granulation, Blending, Compression, Capsule, Coating and Packing as per their respective SOPs and batch records.
• Monitoring & Verifying of Records: – To monitor day to day activity in all area like Days store, Change part room, Quarantine area and Accessory room. Verifying the logbook, environment monitoring record, inward outward record and inventory records of all concern areas.
• In-process Activities: – Perform the in process activities as per the SOPs, BMR and BPR in all concern areas like Compression, Capsule and Packing.
• Sampling: – Doing the sampling at different stages like Blending, Compression, Coating, Capsule and Packing as per the SOPs, BMR and sampling plan.
• Process Validation activities: – Monitoring of the validation batch at different stages and collection of samples as per the protocol.
• Documentation & Calibration: - Maintaining the all documents related to the IPQA like Semi finish sample register, Validation sample register, Rinse water register, control sample register, finish sample register and performing the calibration of the equipment in IPQA.