Process Engineer — Medical Device; Onsite — Maple Grove, MN
Job in
Maple Grove, Hennepin County, Minnesota, 55311, USA
Listing for:
Pharmavise Corporation
Contract
position
Listed on 2026-02-12
Job specializations:
-
Engineering
Quality Engineering, Process Engineer, Manufacturing Engineer, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 85000 - 110000 USD Yearly
USD
85000.00
110000.00
YEAR
Job Description & How to Apply Below
Position: 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 Linked In:
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.
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