Piramal Pharma Ltd
Website:
piramalpharma.com
Company:
https://www.linkedin.com/company/lifeatpiramalpharma
Seniority: Not Applicable
Industries: Pharmaceutical Manufacturing
Job details:
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Job Description
Executive - ProductionJob Description 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 Responsibilities 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. Essential Qualification B. PHARM / B.Sc.Full time
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