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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

• Perform analysis of in-process, intermediate, stability, and hold-time study samples.
• Conduct UV and HPLC analysis as per SOPs and in-house procedures.
• Handle charging and withdrawal of stability samples.
• Prepare stability study protocols and reports.
• Maintain all analytical records and documentation as per cGMP requirements.
• Support investigations related to deviations and Out of Specification (OOS) results.
• Perform reporting authority responsibilities in their absence.
• Work in rotating shifts as required.
• Perform other duties assigned by seniors.