The Manufacturing Process Engineer is responsible for design, project management, and implementation of new and existing systems, utilities and equipment, and ensures Quality, Compliance, and improved OTIF for all products produced at the parenteral/sterile filling manufacturing facility in Lexington, Kentucky.
REQUIRED EXPERIENCE & SKILLS:
3+ years of experience with pharmaceutical manufacturing/maintenance for parenteral/sterile filling
Experience troubleshooting production equipment
Experience with Allen-Bradley ControlLogix and Siemens PLCs
Experience with HMI software applications
Experience with automating processes and equipment
Okay with flexible schedule
DESIRED EXPERIENCE & SKILLS:
BS in Mechanical, Electrical, or Chemical Engineering
Competitive compensation and relocation is available for this position.
Please contact us for additional details and to discuss position.
**NO SPONSORSHIP IS AVAILABLE FOR THIS POSTION**