Executive Qa (ipqa)

Year Mohali, Punjab, India

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Ensure compliance to cGMP for all operational activities.
Monitor the formulated products against stipulated conditions mentioned in the Batch production record.
Conduct certificate of batch production records for compliance and stage wise completion.
Conduct line clearance during manufacturing and the packing activities.
Conduct sampling activities during the manufacturing and the packing activities.
Conduct qualification, PPV, PM and calibration of in-process instruments as per schedule.
Swab and Rinse sampling activity for cleaning validation and verification studies.
Initiate Deviation, Change Control and Investigations.
Provide support to conduct investigations related to deviation, CAPA, OOS, OOT, and Market complaint handling.
Issuance of Batch production records.
Review & Verification of Bin for Documents / Labels Destruction as per SOP.

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