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:

1. 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.

1. May assist in inventing / creating concepts and designs/approaches for new products/processes/test methods.

1. Designs, procures, and fabricates simple tooling and fixtures.

1. Designs and coordinates rudimentary engineering tests and experiments.

1. Applies the Technical Development Process (TDP)/Product Development Process (PDP) methodologies.

1. Prepares standard reports/documentation to communicate results to technical community.

1. Completes basic tasks on engineering documentation.

1. Train technicians/operators on new processes and/or test procedures.

1. 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