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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

Responsibilities:

Strict adherence to cGMP norms and safety rules of the factory. Maintaining the documents relating to SAP clearance activities. Up keeping the stock register for label. Creating the PR for materials required for QC function. Maintaining the stock of chemicals and consumables. Preparing the approved labels as per dispatch requirements. Sending the customer requirement samples, as per marketing requirement. Coordinating with Quality Assurance department in releasing the products. All records and documents should be maintaining as per SOP. Maintaining laboratory systems as per the regulatory requirements.

Qualification: M.Sc. – Chemistry
Experience: 1-3 Years experience