Job Description
Our F500 Medical Device client has an exciting opportunity for an R &D Engineer II.
Job Summary :
Develops products, materials, processes, or equipment for projects of moderate complexity.
Under limited supervision / guidance, compiles, analyzes, and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials.
Key Responsibilities :
Fully participates in and successfully contributes to project teams typically including the following activities : product design and development, test of materials, preparation of specifications, process capability studies, research investigations (animal and clinical studies), report preparation, and process / test documentation.
Works independently to plan and schedule own activities necessary to meet timelines.
Designs and coordinates standard engineering tests and experiments.
Designs, procures , and fabricates tooling and fixtures.
Performs troubleshooting on new products / process problems as related to design, material, or process.
Summarizes, analyzes, and draws conclusions from test results.
Prepares standard reports / documentation to communicate results to technical community.
Responsible for engineering documentation.
Invents / creates concepts and designs for new products / processes and submits idea disclosures.
May train and / or provide work direction to technicians.
Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.
Demonstrates PDP / TPD system knowledge through delivery of high-quality deliverables.
Quality Systems Duties and Responsibilities :
Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
Qualifications :
Engineering or physics degree required
Can accept with Masters - fresh grad (no exp)
2+ years of experience (internship experience will not be considered for # of years of experience)
Hands on lab experience , test methods , testing equipment
MS Office, Operation of equipment & testers
Nice to have (But not required )
Tooling / Fixturing experience.
3D print
Medical Device experience
Other Details :
Schedule : 08 : 00 : AM - 04 : 30 : PM (Flexible on start-end times - must be within core hours )
Work Setup : Onsite in Arbor Lakes , MN
Contract Length : 12 Months ( 1 / 12 / 2026 - 1 / 11 / 2027 )
Requirements
R&D
Engineer Medical Device • Maple Grove, MN, us