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

Job Description Our F500 Medical Device client has an exciting opportunity for a Process Development Engineer.

Job Summary:

Assists in the development and analysis of products, materials, processes, or equipment. Under direct supervision/guidance, compiles, analyzes and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, or materials.

Responsibilities:

Undertakes and successfully completes simple or basic project/product development tasks to include any of the following: writing and/or verifying specifications, maintaining product/process documentation, testing processes, equipment, raw materials and product, and validating equipment and processes. May assist in inventing / creating concepts and designs/approaches for new products/processes/test methods. Designs, procures, and fabricates simple tooling and fixtures. Designs and coordinates rudimentary engineering tests and experiments. Applies the Technical Development Process (TDP)/Product Development Process (PDP) methodologies. Prepares standard reports/documentation to communicate results to technical community. Completes basic tasks on engineering documentation. Train technicians/operators on new processes and/or test procedures. Identifies areas for improvement, suggests solutions, and submits idea records.

Quality Systems Duties and Responsibilities:

Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Qualifications 0 - 1 Year with BS Bachelors of Science/Biomedical/Mechanical Chemical or Material Science preferred

Additional Job Specific Requirements:

Collaborates effectively with cross functional peers.

Other Details:

Schedule:

08:00:

AM - 04:30:

PM Contract Length:

12 months

Work Set-Up:

Onsite in

Maple Grove, MN Start Date:

12/29/2025