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Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.  

This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.  

Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.  

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Job Description

Key Roles/Responsibilities:

• Supervises the line operations and participates in Validation activities as per the protocol.

• Maintains c-GMP practices along with documentation in various records.
• Supervision of Bottle packing line.

• Checks BPR before submission to the superiors..

• Imparts on job/ Classroom training to the workmen for SOP and cGMP systems.

• Monitors and reports the unauthorized movement of workmen from the line.

• Take-up the responsibilities of the immediate supervisor for the section in his absence.

• Preparation of new SOPs and updation of existing SOPs.

• Participate in machine qualification activities.

• Check all the calibration tags of equipment, instruments, and fire extinguishers for their due date time to time.

• Knowledge and involvement in SFTI, OEE, DHM & 5S Activities.

• Knowledge and involvement in ISO 14000 & 13485 and EHS compliance (Near Miss reporting, UA & UC).

• Any other activity from time to time which his supervisor/company feels appropriate.

• Prepare and cross-verify the material return note (MRN) after the completion batch/product campaign.

• Prepare the line rejection note (LRN) wherever required.

• Ensure that error free Batch Records are submitted to QA on time.

• Ensure that no impact on Dispatch plan due to document

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