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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

• To prepare/Review the Annual Product Review (APR) as per the schedule planner.

• Issuance & handling of logbooks for all quality management systems.

• Management of all master documents in manual and electronic format of all the departments.

• Support in internal and external audits of the facility, including compliance.

• Handling of QMS activities and support in investigation, like incident, deviation, change control, etc.

• Management of temperature monitoring data loggers in the control sample and document room.

• Destruction of Control Sample, Batch Records, Logbooks, and other GMP Records as per Schedule.

• Management of Control Sample and Document Room.