Process Development Engineer — Medical Device; Onsite — Maple Grove, MN

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

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

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.

• Undertakes and successfully completes simple or basic project/product development tasks including 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 or 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.
• Builds quality into all aspects of work by maintaining compliance with all quality requirements.

• 0–1 year experience with a BS.
• Bachelor’s degree in Science, Biomedical, Mechanical, Chemical, or Material Science preferred.
• Collaborates effectively with cross‑functional peers.

• Schedule:
  
  08:00 AM – 04:30 PM.
• Work Set‑Up:
  Onsite in Maple Grove, MN.
• Start Date:
  
  12/29/2025.
• Seniority level:
  Entry level.
• Employment type:
  
  Contract.
• Job function:
  Medical Equipment Manufacturing.