Process Engineer

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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.

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Job Title

Job Description

Drafts experimental development and operational studies to expand expertise in parenteral manufacturing.

Ensures that work is performed in an accurate timely and efficient manner and in compliance with company policies SOPs cGMP regulations and FDA regulations.

Contributes to resolving deviations investigations and continuous improvements to improve processes quality costs safety and/or cycle time.

Interfaces with Operations Validation Quality Assurance groups and Formulation Development to identify new components and/or processes into the existing manufacturing environment.

Take initiative to develop and improve procedures and setups through the change control process.

Prepares and reviews technical documents to include but not limited to: Technical Reports SOPs Master Batch Records (MBRs) Change Controls Cost Quotes Product and Process Verification/Validation Protocols.

Contributes to investigations and deviations related to manufacturing defines root causes and implements corrective actions.

Troubleshoots and investigates manufacturing problems monitors the processes and optimizes processes as required.