IPQA

- To give line clearance at relevant stages of process i.e. dispensing, manufacturing and packing stages.
- To perform online in-process activities during manufacturing and packing area as per approved BMRs & BPRs and immediately reporting of any deviation to supervisor.
- To collect and send samples (through LIMS/manually) i.e. routine batches analysis samples from respective stage, retest samples, process, Hold time study and cleaning validation sample as per respective sampling plan to quality control unit.
- Execution of the process validation activities as per approved validation protocol.
- To assist qualification activities as per respective protocol/instructions.
- To collect and handed over the sample in control sample room.
- Collection & submission of stability samples with stability request in QC department.




- To ensure cGMP, GDP and GEP compliances during his shift in his respective area.
- To review batch documents i.e. BMRs and BPRs online at each stage and completion of batch.
- To perform daily, monthly and quarterly and/or as per requirement, verification/ calibration of respective IPQA instruments.
- To monitor the effectiveness of CAPA taken relevant shop floor.
- To verify the rejected consignment at warehouse.
- To issue documents i.e. additional pages of BMRs, BPRs in shift as per requirements.
- To perform the any other task/responsibility assigned by section in-charge.

📌 Officer - Quality Assurance (Baddi)
🏢 USV
📍 Baddi