Process Engineer Medical Device (Onsite Maple Grove, MN) Contract

Process Engineer — Medical Device (Onsite — Maple Grove, MN) Contract Maple Grove, United States | Posted on 12/09/2025 From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at and follow us on LinkedIn: Job Description Our F500 Medical Device client has an exciting opportunity for a Process Engineer. Job Summary Leads clinical build line, own process development deliverables such as process validation documentation, characterize process, support commercialization activity. Key Responsibilities Works cooperatively with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain, and Marketing on complex projects to ensure project success. Consistently generates innovative and unique solutions to meet department goals. Successfully completes complex engineering work and contributes to new product development teams and product support, typically including the following activities: technology development, test of materials or products, preparation of specifications, Six Sigma, process study, process improvements, and report preparation. Selects process improvement techniques to solve complex problems and make sound equipment and process recommendations. Summarizes, analyzes, and draws conclusions from complex test results. Designs and prepares complex reports and communicates results to the technical community. Designs and coordinates complex engineering tests and experiments. Coordinates, manages, and documents project goals and progress and recommends appropriate revisions. Assess the feasibility and soundness of proposed engineering evaluation tests, products, or equipment. Completes and manages complex Capital Equipment Request Authorizations (CERA’s). Leads cross-functional project teams. Leads in the identification, implementation, and management of production goals. Trains, develops, and/or provides work direction to operators, technicians, and engineers. Quality Systems Duties and Responsibilities Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Qualifications 5+ years of experience Additional Job Specific Requirements Knowledge of electropolishing Experience with Keyance and Sensofar measurement technology Other Details Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment. #J-18808-Ljbffr