<Back to Search
Process Engineer III - Medical Device (Onsite - Maple Grove, MN) Contract
Maple Grove, MNMarch 31st, 2026
Job DescriptionOur F500 Medical Device client has an exciting opportunity for a Process Engineer III.Job Summary:Develops new technology, products, materials, processes, or equipment with minimal supervision. Independently, or as a member of a team, develops, directs, and executes plans for a major segment of complex projects. Compiles and analyzes operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials.Key Responsibilities:Consistently generates innovative and unique solutions to market needs and submits idea disclosures. Work is expected to result in the development of new or refined products, processes or equipment.Successfully completes complex engineering work in one or more of the following: technology development, product design and development, test of materials or products, preparation of specifications, process study, research investigation (animal and clinical studies), and report preparation.Selects techniques to solve complex problems and make sound design recommendations.Summarizes, analyzes, and draws conclusions from complex test results.Designs and prepares complex reports to communicate results to technical community.Designs and coordinates complex engineering tests and experiments.Coordinates, manages, and documents project goals and progress and recommends appropriate revisions.Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment.Interfaces with Physicians/Cath Lab personnel to obtain feedback on concepts and performance of new devices.Translates customer needs into product requirements and design specifications.Responsible for engineering documentationWorks cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success.May train and/or provide work direction to technicians and entry-level engineers.Demonstrates PDP/TPD system knowledge through delivery of high quality and high impact deliverables.Quality Systems Duties and Responsibilities:Build Quality into all aspects of their work by maintaining compliance to all quality requirements.Qualifications:3 - 5 Years with BSAdditional Job Specific Requirements:1. Able to collaborate effectively with cross functional peers2. Prior experience in a regulated industry3. Prior experience with manufacturing and/or process developmentOther Details:Schedule: 08:00:AM - 04:30:PMWork Setup: Onsite 5 days per week in Maple Grove, MN
Showing all 21,387 matching similar jobs
- Senior Manufacturing Engineer(Medical Device)-- MEHDC5774463
- Software QA Engineer II - Medical Devices Remote
- Manufacturing Engineer - Medical Devices
- Sr Process Development Engineer- Med Device- Mount Laurel, NJ
- Software Engineer(Medical Devices)
- Senior Process Development Engineer - Medical Device
- QA Test Manager - Boston, MA
- Product development engineer (Imaging optimization)
- Manufacturing Process Engineer-Medical Device
- Remote Sr. Quality Systems Engineer – eCOC & Regulatory
- SAP test lead
- Facets QA Test Lead
- Senior Test Engineer
- Biomedical Engineer
- Project Engineer - Advanced Resistive Exercise Device (ARED)
- Senior Process Engineer II
- Medical Device Packaging Design Engineer
- Module Development Engineer
- Test Technician, Senior
- Field Process Engineer 4
- BDM _ Product Engineering, Med Devices
- EET GSEP Technical Test 6117854
- Collateral Device Engineer
- Engineer
- Engineer, Complaints Technical Investigator, Medical Devices (JP15046)
- Medical Device Senior Manufacturing Engineer
- EET GSEP Technical Test 6117854
- Lead Manufacturing Engineer - Medical Device - Woburn, MA
- Senior Medical Device Safety Engineer
- Senior Manager, Device & Combination Product Design
- Staff Product Safety Engineer - Medical Device
- Senior Test Engineer
- Medical Device Packaging Design Engineer
- Software Systems Engineer (exp in Medical device)
- Contract QA Test Lead
- GXP Test Lead
- Senior Software Requirements & Systems Engineer (Medical Devices) (Hybrid - Acton, MA or San Di[...]
- Senior Medical Device Software QA Engineer
- Senior Spine Device Engineer - CREO, FDA & Leadership
- Senior R&D Engineer - Medical Device (Onsite - Maple Grove, MN) Possible Temp-to-Hire