The Role
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.
Summary Generated by Built In
Be the First to Apply
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 timeSkills Required
- B. Pharm or B.Sc. degree
Am I A Good Fit?
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.
Success! Refresh the page to see how your skills align with this role.
The Company
What We Do
Piramal Pharma Limited is a global pharmaceutical company that provides end-to-end drug development and manufacturing services (CDMO), complex hospital generics, and consumer healthcare products.

.png)






