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

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 mo nths Work Set-Up: Onsite in Maple Grove, MN Start Date: 12/29/2025