Minimum experience required in this position:
Preparing, reviewing, and executing Process Validation, Hold time study protocol and cleaning validation protocol with its reports.
Sampling as per Process Validation, Hold time study protocol and cleaning validation protocol.
Reviewing and monitoring all the activities related to documentation of Production and QC department.
Reviewing of BMR/BPR and Logbook.
Facing audits like USFDA, MHRA, and TGA etc.
Reviewing of logbooks of IPQC instruments and its calibration records.
Monitoring in-process checks in granulation, compression, coating, cream manufacturing, tube filling and packing area.
Division : - Pharma Formulation (OSD and External Preperation)