Process Engineer — Medical Device (Onsite — Maple Grove, MN) Contract
On-siteMaple Grove, Minnesota, United States
Job Summary
Lead clinical build lines and own process development deliverables including process validation documentation and characterization. Collaborate cross-functionally with R&D, Quality, Production, and Regulatory teams to execute complex engineering work, new product development, and Six Sigma process studies. Select improvement techniques to solve problems, analyze test results, and design experiments while managing Capital Equipment Request Authorizations. Train operators and technicians, coordinate project goals, and communicate findings to the technical community. Maintain full compliance with quality requirements throughout all activities.
Required Qualifications
- 5+ years of experience", "BS in engineering (Mechanical, Chemical, BioMed)", "Knowledge of electropolishing", "Experience with Keyance and Sensofar measurement technology
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