Trainee - QC

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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

Trainee - QC

Job Description

Responsible for testing and release of In process & product changeover equipment cleaning samples received on daily basis. Daily verification of analytical / precision balances & KF titrators.

1. Strict adherence to cGMP norms and safety rules of the factory.
2. Receiving and inwarding the Inprocess and product changeover equipment cleaning samples received from all the production blocks. 
3. Testing and release of all the received Inprocess and equipment changeover cleaning samples on time without delay.
4. Ensuring the availability of working / reference standards required to perform the cleaning sample analysis as per product changeover MACO sheets.
5. Timely intimating the receipt of Inprocess sample w.r.t HPLC/GC analysis to respective shift executive for prompt completion of testing and release.
6. Timely collection, testing and release of Swab samples associated with product changeover equipment cleaning samples. 
7. Supporting for Sampling and testing of Raw materials, packaging materials, Intermediates and Finished product upon demand. 
8. Coordinating with stakeholders for smooth functioning of IPQC section. 
9. Ensuring the contemporaneous documentation for the activities being done in RM section in the corresponding logbooks / inward registers / check lists / analytical testing protocols / raw data sheets.
10. Maintaining the records and documents as per SOP.