Supervises production quality of tablets and capsules while ensuring compliance with c-GMP and safety standards. Responsibilities include manpower allocation, operation oversight, machine qualification, documentation maintenance, and training of staff.
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Job Description
Senior Executive - ProductionAny other activity from time to time which his supervisor/company feels appropriate. Supervises quality products are being manufactured (Tablets and Capsules Inspection) in conformance with c-GMP / Safety and hygiene requirements on shift-to-shift basis. Maintains overall disciplines and productivity. Key Roles/Responsibilities: • Allocates workmen for different workstations on shift-to-shift basis. • Ensure no stoppage of operation / machines due to non-availability of manpower and any kind of machine breakdown. • Supervises the line operations and participate in Validation activities as per the protocol. • Maintains c-GMP practices along with documentations in various records. • Fills and checks BMR / BPR before submission to the superiors. • Handles minor parametric setting issues in various machines and products. • Monitors speed of machine and output according to the run time. • Imparts on job / Classroom training to the concern workmen and supervisor for SOP and cGMP systems. • Imparts induction activity to all new joining. • Monitors and reports the unauthorized movement of workmen from line. • Takes up the responsibilities of the immediate supervisor for the section in his absence. • Helps section in charge in preparation of SOP. • Verifies the balances on daily and monthly basis. • Participate in machine qualification activities. • Checks all the calibration tags of equipment, instruments, or fire extinguisher for their due date time to time. • Knowledge and involvement in EHS, SFTI & 6S Activities. • Knowledge and involvement in ISO 14000 & 13485. • Any other activity from time to time which his supervisor / company feels appropriate. • Checking of line clearance during batch change over. • In process testing as defined in Batch Manufacturing Record. • Approval of Material Return Note (MRN), Material Requisition Note (MRQN), Line rejection Note (LRN) of Processing area. • Review the Batch Manufacturing and other quality documents. • To perform challenge test as per the BMR / SOP with define frequency. B. PHARM / B.Sc.Full timeSimilar Jobs
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