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.

2. 
   May
   assist
   in inventing / creating concepts and designs/approaches for new products/processes/test methods.

3. 
   Designs,
   procures
   , and fabricates simple tooling and fixtures.

4. 
   Designs and coordinates rudimentary engineering tests and experiments.

5. 
   Applies the Technical Development Process (TDP)/Product Development Process (PDP) methodologies.

6. 
   Prepares standard reports/documentation to communicate results to
   technical
   community.

7. 
   Completes basic tasks on engineering documentation.

8. 
   Train technicians/operators on new processes and/or test procedures.

9. 
   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