Piramal Pharma is inviting applications for the role of Executive-Production at Piathampur,MP. This production role is focused on compression area operations, c-GMP compliance, documentation, safety practices and shift-wise supervision of manufacturing activities.
| Company | Piramal Pharma |
| Division | Piramal Pharma Solutions |
| Position | Executive-Production |
| Department | Production |
| Location | Piathampur,MP |
| Employment Type | Full time |
Job Description
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. The Executive-Production role involves supervising compression activity to ensure quality products are manufactured in conformance with c-GMP, safety and hygiene requirements on a shift-to-shift basis. The role also includes maintaining discipline and productivity in the production area.
Key Responsibilities
- Allocate workmen for different workstations on a shift-to-shift basis.
- Supervise line operations including weight verification, product recipe selection, machine setting, initial parameter setting, in-process checks, product challenge test, metal detector challenge test and rejection verification challenge test during compression operations.
- Review batch manufacturing records and other quality documents.
- Fill process parameters, Batch Manufacturing Record (BMR) and GMP documents or records as required by following ALCOA+ principles.
- Ensure there is no stoppage of operations or machines due to non-availability of manpower or machine breakdown.
- Participate in validation activities such as Equipment/Area and Trial/Study/Pre-exhibit/Exhibit/validation batch activities as per protocol.
- Maintain c-GMP practices along with documentation in various records.
- Handle minor parametric setting issues in various machines and products.
- Monitor machine speed and output according to run time.
- Monitor and report unauthorized movement of workmen from the line.
- Take up the responsibilities of the immediate supervisor for the section in his absence.
- Support the section in charge in preparing SOP and other GMP documents.
- Report day-to-day activities in the SAP system, if SAP user ID is available.
- Carry out verification/calibration of balances, timer, load cell, encoder, filling depth, timer synchronization and related items on a daily/monthly basis or as required.
- Participate in machine qualification activities as per qualification protocol whenever required.
- Check calibration/qualification tags of equipment, instruments or fire extinguishers for due dates from time to time.
- Check line clearance during product changeover and batch changeover, and monitor temperature, RH, pressure gradient, area cleaning and disinfections.
- Be involved in EHS, SFTI, 6S, ISO 14001 and 13485 activities.
- Fill safety checklist, provide tool box talk training, and report unsafe condition, unsafe act and learning incident (near miss).
- Perform and ensure activities are carried out as per hazard identification and risk assessment (HIRA) and site EHS procedure (SEP).
- Provide training to subordinates as and when required.
- Perform any other activity from time to time that the supervisor/company feels appropriate.
How to Apply
Interested candidates can apply online through the official Piramal Pharma Workday application link given below.


