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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, and stability samples as per SOPs.
• Conduct UV and HPLC analysis in rotational shifts.
• Handle stability sample charging, withdrawal, and analysis.
• Prepare stability protocols and reports.
• Perform hold-time study sample analysis.
• Maintain analytical records and documentation as per cGMP requirements.
• Support investigations of deviations and Out of Specification (OOS) results.
• Handle reporting authority responsibilities in their absence.
• Perform additional responsibilities as assigned by seniors.