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Process Engineer III - Medical Device; Onsite - Maple Grove, MN

Job in Maple Grove, Hennepin County, Minnesota, 55311, USA
Listing for: Pharmavise
Contract position
Listed on 2026-06-02
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Manufacturing Engineer, Biomedical Engineer
Job Description & How to Apply Below
Position: Process Engineer III - Medical Device (Onsite - Maple Grove, MN) Contract
Job Description
Our 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 documentation
  • Works 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 BS

    Additional Job Specific Requirements:

    1. Able to collaborate effectively with cross functional peers

    2. Prior experience in a regulated industry

    3. Prior experience with manufacturing and/or process development

    Other Details:

    Schedule:

    08:00:

    AM - 04:30:

    PM

    Work Setup:
    Onsite 5 days per week in Maple Grove, MN

    Contract Duration: 12 Months (1/5/2026 - 1/4/2027)
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