This position is a key role in the Injection Molding Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Injection Molding Operations. You will also be involved in Cross-functional project management within this role. Cleveland’s technology and automation is cutting edge. It is the U.S. sole source for plastic pour bottles, glass IV bottles, and various reconstitution devices. This facility produces several major product lines with a diverse array of automated manufacturing technologies ranging from bottle solution filling, injection molding, tubing extrusion, and device assembly. Our Cleveland plant has been an integral part of Baxter for over 70 years. The work is challenging and rewarding, as Baxter offers competitive compensation and benefits. Baxter encourages and values every employee and believes that all can make contributions toward advancing healthcare for patients; work to be proud of. What we offer from Day One Medical, Dental and Vision coverage 160 hours of Paid Time Off and Paid Holidays 401K match Employee Stock Purchase Program Paid Parental Leave Tuition Reimbursement What you'll be doing Design/modify precision medical molding & inspection equipment. Manage multiple projects with minimal supervision. Prepare estimates for various tasks and projects. Manage capital projects both directly and through coordinating engineers. Drive Continuous Improvement Activities. Work with plant and corporate groups as well as contractors and vendors. Manage start-up, debug, and commission of new manufacturing processes. Equipment life cycle management including upgrades, replacement, and decommissioning. Product life cycle management including product design changes, material changes, Supplier Notice of Change (SNC) assessments, specification changes, etc. Provide technical support/troubleshooting to injection molding operations. Demonstrate proactive communication and problem solving. Responsible for supporting and achieving Value Improvement Projects (VIP’s). Responsible for adhering to FDA Design Control standards at all times. Adhering to and maintaining all department Standard Operating Procedures (SOPs), forms, and logbooks. Generate technical documents, reports, equipment specifications, and interpret technical drawings/schematics.

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