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Process Engineer

Piramal Pharma Ltd
Posted 3 months ago, valid for 13 days
Location

Lexington, KY 40546, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Piramal Pharma Solutions is seeking a Process Engineer II to design and optimize manufacturing processes in compliance with industry regulations.
  • The role involves drafting operational studies, resolving deviations, and collaborating with various departments to enhance manufacturing efficiency.
  • Candidates should possess a Bachelor of Engineering in Chemical and have at least 3 years of relevant experience in a similar role.
  • The position requires strong problem-solving skills and the ability to prepare technical documents such as SOPs and validation protocols.
  • The salary for this role is competitive and commensurate with experience.

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing聽 organization (CDMO), offering end-to-end development and manufacturing聽 solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.聽聽

This enables us to offer a comprehensive range of services including Drug Discovery聽 Solutions, Process & Pharmaceutical Development services, Clinical Trial聽 Supplies, Commercial supply of APIs and Finished dosage forms. We also offer聽 specialized services like development and manufacture of Highly Potent APIs聽 and Antibody Drug Conjugation.聽聽

Our capability as an integrated service provider聽 & experience with various technologies enables us to serve Innovator and聽 Generic companies worldwide.聽聽

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Process Engineer II

Job Description

The Process Engineer works to design and efficiently transfer new processes into manufacturing, optimize existing processes, ensuring the achievement of quality, yield, and capacity timelines.

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

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

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

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

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

路 Prepares and reviews technical documents to include but not limited to: Technical Reports, SOP's, Master Batch Records (MBR's), Change Controls, Cost Quotes, Product and Process Verification/Validation Protocols.

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

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

Bachelor of Engineering (Chemical), English



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