Production and Packing planning, Monitoring and reporting daily Production Activities, Master Creation In Pharma Cloud, SAP. IPQA, Document Issuance & Control, CSV, Stability, Validation
To Review Qualification Protocol and Reports of Equipment, Instrument, System.To Review Qualification Protocol and Reports of Computer System Validation CSV. Ensuring safe handling of Raw Materials and Packing Materials. Dispensing activity of RM and PM material.
Should have sound knowledge of BFS machine operation, aseptic area, maintenance, media fill, batch mfg., CIP, SIP, Autoclave, topical manufacturing. Candidate having experience in different packing lines of OSD & sterile manufacturing.
B.Pharm/M.Pharm/B.Sc/M.Sc; Production and Packaging, Planning, Monitoring and Reporting production activities. Purchase and procurement planning, monitoring and reporting purchase activities
Collecting and submitting in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples as per the respective procedures, batch manufacturing records and packing records, protocols. Conducting AQl inspections and periodic inspections of control samples
Planning and performance of Validation, Verification of analytical methods as per the relevant procedures, protocols. Experience in Handling of GC, HPLC, IC, UV instruments with Lab solutions, Empower, Chromelon, Magic net software and experience on LIMS.
Glenmark Pharmaceuticals Limited is a research‐led, global pharmaceutical company, having a presence across branded, generics, and OTC segments; with a focus in the therapy areas of Respiratory, Dermatology and Oncology.