AstraZeneca seeks a Process Engineer for its Coppell, Texas manufacturing facility to work 12-hour day shifts. The role involves leading process improvements, designing studies, managing equipment installations, and ensuring compliance with Good Manufacturing Practices in a pharmaceutical production environment.
Responsibilities
- Lead and implement process improvements to enhance safety, quality, yield, and cost efficiency
- Develop conceptual strategies, feasibility studies, and detailed scopes for process projects
- Design and execute experiments, analyze data, and author technical reports and proposals
- Author, review, and approve procedures and batch records for GMP compliance
- Support equipment commissioning activities including FATs, SATs, IQ, OQ, and PQ
Requirements
- Bachelor of Science in Chemical Engineering or related technical discipline
- 1-2 years pharmaceutical or GMP-regulated manufacturing experience
- Proficiency reading P&IDs, process flow diagrams, mass and energy balances
- Strong verbal, written, and interpersonal communication skills
- Experience with batch reactors, filter dryers, vacuum systems, and heat exchangers
- PLC/SCADA or DCS control systems knowledge at operational or engineering level
Process Engineer - Day Shift in coppell at Unknown Company
This position is listed as full time and onsite.