2-3

MDl, lnhalers, Nasal, Manufacturing, Filling and Packing, Dispensing, Dispatch, PassX, QMS

Having good experience of method development on HPLC and GC instruments and other analytical instruments. Having knowledge of wet analysis

Environmental monitoring of manufacturing clean room area. Non-viable particle monitoring of manufacturing clean room area. Personnel monitoring. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g. plates, swabs, etc.

Candidates with experience in handling of sophisticated instruments e.g. HPLC, GC, UV, IR, Dissolution apparatuses and other laboratory equipment are preferred.

Exposure of QMS activities Exposure of Ampho, Bupivacaine Autoclave Operation and Supervision Lyo Operation and Supervision Regulatory Audit exposure Online documentation of BMR and log books during execution of batches

In-Process, FG and Stability, Analytical Instrumentation - HPLC, UV and Dissolution

D.Pharm, B.Pharm, M.Pharm with Gujarat State Pharmacy Council Drug License.

Candidate should have knowledge of packing operations. Knowledge of BQS, Autocarnator and Bottle packing. Responsible to adherence cGMP guidelines.

To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods.