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

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

Maple Grove, United States | Posted on 12/06/2025

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at  and follow us on Linked In:

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 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.

• Schedule:
  
  08:00:
  
  AM - 04:30:
  
  PM
• Work Set-Up:
  Onsite in Maple Grove, MN
• Start Date:
  
  12/29/2025

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.