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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 finished products, in-process samples, intermediate samples, stability samples, and miscellaneous samples as per pharmacopeial, customer, and in-house specifications.
• Operate, calibrate, and maintain QC laboratory instruments, including Amino Acid Analyzer, HPLC, analytical balances, and other analytical equipment.
• Conduct wet chemistry analysis of finished product samples.
• Prepare, maintain, and review laboratory documentation in compliance with cGMP requirements.
• Ensure adherence to laboratory safety procedures and EHS guidelines during all QC activities.
• Handle responsibilities of the reporting manager/supervisor during their absence, as assigned.
• Support routine laboratory operations and undertake additional tasks assigned by senior management.
• Ensure compliance with quality systems, SOPs, and regulatory requirements.
• Contribute to maintaining data integrity and accuracy of analytical results.
• Participate in continuous improvement and laboratory efficiency initiatives.