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Piramal Pharma Solutions

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

Senior Executive-QC

Job Description

Responsible for performing quality control analysis of finished products, in-process, intermediate, miscellaneous, and stability samples in accordance with pharmacopoeial standards, in-house specifications, customer requirements, and cGMP guidelines. Operates, handles, and calibrates laboratory instruments such as UV, HPLC, SOR, and analytical balances, performs wet chemical analysis, maintains accurate QC documentation, ensures compliance with laboratory safety practices, supports departmental operations by acting in the reporting authority's absence when required, and undertakes additional responsibilities assigned by senior management.

1. Analysis of finished products, in-process samples, intermediate samples, miscellaneous samples, and stability samples as per pharmacopoeial requirements, in-house specifications, and customer specifications.

2. Operation, handling, and calibration of UV, SOR, HPLC, analytical balance, and other instruments in the QC laboratory as per requirements.

3. Performance of wet analysis of finished product samples.

4. Maintenance of documentation in compliance with cGMP requirements.

5. Adherence to safety norms in the Quality Control laboratory during all activities.

6. Handling the responsibilities of the reporting authority in his/her absence.

7. Carrying out any other work allocated by seniors.