R&D Engineer II — Medical Device (Onsite— Maple Grove, MN) Possible Temp-to-Hire
Pharmavise Corporation
Office
Maple Grove, United States
Temporary
Our Fortune 500 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.
Responsibilities and Job Requirements:
Key Responsibilities
1. 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.
2. Works independently to plan and schedule own activities necessary to meet timelines.
3. Designs and coordinates standard engineering tests and experiments.
4. Designs, procures, and fabricates tooling and fixtures.
5. Performs troubleshooting on new products/process problems as related to design, material, or process.
6. Summarizes, analyzes, and draws conclusions from test results.
7. Prepares standard reports/documentation to communicate results to technical community.
8. Responsible for engineering documentation.
9. Invents/ creates concepts and designs for new products/processes and submits idea disclosures.
10. May train and/or provide work direction to technicians.
11. Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.
12. 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
2 - 4 Years with BS degree in ME or Bioengineering
Molded component development preferred. CAD experience is a must.
MS Office
PDP/TPD system knowledge
Other Details:
• Schedule: 08:00:AM - 04:30:PM CST
• Contract Length: 12 Months, with possible temp-to-hire for the right candidate.
• Work Set-Up: Onsite in Maple Grove, MN
• Start Date: 9/15/2025
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.
Responsibilities and Job Requirements:
Key Responsibilities
1. 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.
2. Works independently to plan and schedule own activities necessary to meet timelines.
3. Designs and coordinates standard engineering tests and experiments.
4. Designs, procures, and fabricates tooling and fixtures.
5. Performs troubleshooting on new products/process problems as related to design, material, or process.
6. Summarizes, analyzes, and draws conclusions from test results.
7. Prepares standard reports/documentation to communicate results to technical community.
8. Responsible for engineering documentation.
9. Invents/ creates concepts and designs for new products/processes and submits idea disclosures.
10. May train and/or provide work direction to technicians.
11. Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.
12. 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
2 - 4 Years with BS degree in ME or Bioengineering
Molded component development preferred. CAD experience is a must.
MS Office
PDP/TPD system knowledge
Other Details:
• Schedule: 08:00:AM - 04:30:PM CST
• Contract Length: 12 Months, with possible temp-to-hire for the right candidate.
• Work Set-Up: Onsite in Maple Grove, MN
• Start Date: 9/15/2025
R&D Engineer II — Medical Device (Onsite— Maple Grove, MN) Possible Temp-to-Hire
Office
Maple Grove, United States
Temporary
August 19, 2025