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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, intermediate, stability, and miscellaneous samples as per pharmacopeial, in-house, and customer specifications.
• Operate and calibrate QC laboratory instruments such as HPLC, Amino Acid Analyzer, analytical balances, and other laboratory equipment.
• Conduct wet chemical analysis of finished product samples.
• Maintain laboratory records and documentation in compliance with cGMP requirements.
• Follow all safety procedures and guidelines within the Quality Control laboratory.
• Take charge of reporting authority responsibilities during their absence, when required.
• Carry out additional tasks and assignments delegated by management/seniors.