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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

Key Roles/Responsibilities:

• Execute defined procedures to manufacture high potency ADC/ API’s product in support of launched products and clinical trial programmed to GMP standards.
• Working effectively in an organized manner in order to adhere to the planned schedule
• Contribute effectively to a team working environment but also have the ability and confidence to work on an individual basis within the production team.
• Accurately recording information required for batch records
• Updating and reviewing plant documentation, from PI Sheets to SOP’S.
• Maintain high ESH Standards, carrying out all work in accordance with appropriate EHS systems.
• Have a working knowledge of risk management systems and procedures enabling escalation of deviation as appropriate.
• Demonstrate flexibility, self-control, and interpersonal awareness within the team environment.