Antibodies, Application Programming Interface (API), Biotech and Pharmaceutical, Change Control, Chemical Engineering, Clinical Trial, Continuous Improvement, Contract Manufacturing, Corporate Compliance, Corporate Policies, Corrective Action, Cost Control, Current Good Manufacturing Practice (cGMP), Dosage Forms, Drug Development, Drug Discovery, English Language, FDA Requirements, Identify Issues, Manufacturing, Medical Products, Network Integration, Procedure Development, Process Engineering, Process Improvement, Process Manufacturing, Process Validation, Product Costing, Quality Assurance, Quality Management, Safety/Work Safety, Standard Operating Procedures (SOP), Technical Writing, Time Management, Validation Plan, Validation Testing
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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
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.
- 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, SOP's, Master Batch Records (MBR's), 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.
Bachelor of Engineering (Chemical), English