| Location | Maple Grove, Minnesota |
| Website | http://www.pharmavise.com |
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 months
Work Set-Up: Onsite in Maple Grove, MN
Start Date: 12/29/2025