Job Description

Our Fortune 500 Medical Device client has an exciting opportunity for a Senior Process Engineer.

Job Summary:

Independently conducts development work as part of a major research and/or development project. Receives minimal technical direction/review on broad scope or complex projects. Viewed as an expert in one or more in-house technologies.

Responsibilities and Job Requirements:

Drives complex or novel assignment requiring the development of new or improved techniques and procedures. Work is expected to result in the development of new or refined technologies, products, materials, processes, equipment, and/or scientific method to broaden client's Intellectual Property in key strategic areas.

Successfully completes engineering work in one or more of the following: technology development, product design and development, test of materials, preparation of specifications, process study, research investigation (animal and clinical studies), and report preparation.

Provides guidance to product and technology teams.

Assesses the feasibility and soundness of alternative engineering processes, products, or equipment.

Coordinates, manages, and documents project goals and progress and recommends appropriate revisions.

Develops and coaches others on engineering documentation.

Trains and/or provides work direction to technicians and less experienced engineers.

Leads engineering teams to the successful completion of project goals.

Demonstrates PDP/TPD system knowledge through coaching and delivery of high quality, high impact deliverables.

Quality Systems Duties and Responsibilities:

Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

Qualifications

9 - 13 Years with BS, 7 - 11 Years with MS, 4 - 8 Years with PhD

Has a strong understanding of test method development processes, and sterilization and aging protocols for medical devices.

Leverages experience working through med. device quality systems to accelerate project delivery.

Test Method Process methodologies experience required.

Additional Job Specific Requirements:

Leads test method development for conditioned testing on novel medical devices and sub-assemblies

Other Details:

Schedule: 40 hrs/week

Contract Length: 12 months

Work Set-Up: Onsite in Maple Grove, MN

Start Date: 12/2/2025

Job Tags

Full time, Contract work,

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