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Piramal Pharma Solutions

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

Senior Executive

Job Description

Responsible for analysis of in-process, intermediate, finished product, stability, working standard, and impurity standard samples as per pharmacopoeial, in-house, and customer specifications. The role involves preparation, validation, inventory management, and maintenance of working and reference standards, along with ensuring cGMP-compliant documentation and timely execution of assigned analytical activities. Also responsible for supporting departmental operations and handling reporting responsibilities in the absence of the reporting authority.

Supports Quality revenue generation by timely supply of working standard, primary reference standard and impurity standard along with API samples.

• Perform analysis of in-process, intermediate, and finished product samples as per pharmacopoeial, in-house, and customer specifications.
• Conduct analysis of working standards and impurity standards.
• Procure and maintain inventory of primary reference standards and working standards.
• Perform sampling and analysis of stability samples as per approved procedures.
• Prepare and validate working standards for finished products as per requirements.
• Maintain proper stock and inventory records of working and impurity standards.
• Prepare new lots of working standards as required.
• Maintain all analytical documentation and records in compliance with cGMP requirements.
• Handle reporting authority responsibilities in their absence.
• Perform other tasks and responsibilities assigned by seniors.
• Supports Quality revenue generation by timely supply of working standard, primary reference standard and impurity standard along with API samples.