REQ Solutions
Job Title: Process Engineer - Medical Device
Duration: 12+ Months (Possible extension)
Location: Maple Grove, MN 55311
Onsite Role
Responsibilities: Looking for someone with Biomed or ME engineering degree Develops products, materials, processes, or equipment for projects of moderate complexity. 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, 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. May train and/or provide work direction to technicians. Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.
Education/Experience: 2 - 4 Years with BS 0 - 2 Years with MS, preferably in Biomed or ME degree, with industry experience Must have Statistical data analysis Must have Risk documentation experience
Preferred: Interest in team leadership position Openness to mentorship from more experienced engineers
Responsibilities: Looking for someone with Biomed or ME engineering degree Develops products, materials, processes, or equipment for projects of moderate complexity. 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, 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. May train and/or provide work direction to technicians. Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.
Education/Experience: 2 - 4 Years with BS 0 - 2 Years with MS, preferably in Biomed or ME degree, with industry experience Must have Statistical data analysis Must have Risk documentation experience
Preferred: Interest in team leadership position Openness to mentorship from more experienced engineers