Why This Role Stands Out
This hybrid role offers a fantastic opportunity to drive impactful projects and refine manufacturing processes, perfect for a detail-oriented Senior Process Engineer eager to collaborate across teams and leverage their validation and troubleshooting skills. You'll gain valuable experience in GMP environments and contribute to critical product transfers, all while enjoying a competitive hourly rate.
Quick Overview
Job Description
Location: Kalamazoo, MI Salary: $55.00 USD Hourly - $60.00 USD Hourly Description: Our client is currently seeking a Senior Engineer, Process Engineering for a 12 month + contract. Medical, dental, and vision insurance are available to qualified candidates who meet eligibility requirements. This role would spend much of the day supporting process validation activities by running samples on manufacturing equipment, collecting and analyzing data, and documenting results in validation reports.
They would work closely with Quality, Operations, and Engineering teams to ensure processes meet requirements. In addition, they would help set up components, fixtures, tooling, and equipment on the assembly line, troubleshoot issues during builds, and support process improvements as products move into production. Assist and collaborate with materials team to make sure the line is set up to receive components/raw materials.
Overall, the position combines hands-on manufacturing support with technical documentation and cross-functional collaboration
The role contributes to the delivery of high impact, cost transformative projects. The role will require the successful candidate to operate across a network of stakeholders from Product Transfer, Operations and Divisional partners, therefore strong interpersonal skills and communication skills will be necessary. Position will require PPAP skills, analyze equipment to establish operating data, conduct experimental test and result analysis.
May lead or act as independent reviewer in process review meetings. Participate in PFMEA, Control Plan, SOP, PPAP and other Stryker internal process qualification generation associated with product transfers. Ensure adherence to GMP and safety procedures. Equipment Validation Experience. Statistical methods for process development.
Manufacturing/Test Equipment Integration & Troubleshooting
PPAP experience, ability to manage a workstream and its tasks, Complex problem solving,Six Sigma/continuous improvement
Engineering degree, 4 years experience
Medical industry experience STRONGLY preferred
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Contact
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