Executive-production

1 week ago


Dhar, India Piramal Pharma Solutions Full time

**Key Roles/Responsibilities**:

- Allocates workmen for different workstations on shift-to-shift basis.
- Ensure no stoppage of operation / machines due to non-availability of man power 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 in process parameters & manufacturing documentations.
- Involvement in the manufacturing and documentation of Pilot batches in the existing Pilot plant in conformance with cGMP.
- Involvement in the manufacturing and documentation of trial/pre exhibit/ exhibit /commercial batches.
- Fills and checks BMR 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.
- Checks the compressed tablets/coated tablets/filled capsules randomly. If any discrepancy is observed, reports to superiors.
- Monitors and reports the unauthorized movement of workmen from line.
- Takes up the responsibilities of the immediate supervisor for the section in his absence.
- Verifies the balances on daily and monthly basis.
- Participate in machine qualification activities.
- Checks all the calibration tags of equipment, instruments and fire extinguisher for their due date time to time.
- Knowledge and involvement in SFTI & 5S Activities.
- Knowledge and involvement in ISO 14000 & 13485.
- Any other activity from time to time which his supervisor / company feel appropriate.
- Checking of line clearance during batch change over.
- In process testing as defined in Batch Manufacturing Record.
- Perform summary after completion of sub-process like compression and coating.
- Review quality document.


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