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To perform IPQA activities at the shop floor in each and every stage of OSD manufacturing and packing.
QA overview for clean room behavior and aseptic activity.
Review of batch processing records.
Review of all documents relating to the manufacturing Packaging & analysis report prior to batch release.
Review of documents of respective areas and logbooks for adequacy and completeness.
QA overview for receipt of material from warehouse to production.
IPQA of Dispensing Manufacturing Packaging and Dispatch activities.
Review and Control of SOPs Specification BPR issuance Master Formulae and Records.
Preparation & Review of process validation protocols and reports.
Executing the validation/revalidation activity in the absence of an authorized person.
Any job activity assigned by HOD
Handling of the instrument calibration like Balance DT Friability etc.
Additional information
Experience : 12 years (Must have exposure of OSD)
CTC Upto 20k pm.
Industry Type :Pharmaceutical
Functional Area :IPQA
Education :M.Sc or B.Pharm or M.Pharm
Department :Quality Assurance
Regards
Full-Time