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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

• Responsible for the review of In-process analytical data before release.

• Responsible for the review of Intermediates, stability batches and Finished products before release.

• Responsible for the release of Intermediates and finished products.

• Responsible for the review of System audit trails of the instruments in QC.

• Verification of various logbooks for completeness in QC area.

• Responsible for the invalidation of the analytical data.

• Identify and report the potential areas of contamination/Cross contamination.

• Verifying the SOP’s compliance in shop floor.

• Carry out the audits as and when required for laboratory system compliances.

• Report any incident/accident/near miss to the superiors.