R&D Engineer II — Medical Device (Onsite — Maple Grove, MN) Contract – Poss at Pharmavise Corporation

Maple Grove, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

28 Dec, 25

Salary

0.0

Posted On

29 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Product Design, Medical Device Development, Design Controls, Risk Management, Root Cause Analysis, Troubleshooting, Process Capability Studies, Quality Compliance, Engineering Documentation, Test Results Analysis, Project Management, Technical Communication, Team Collaboration, Failure Mode Investigation, Specification Preparation, Process Testing

Industry

Business Consulting and Services

Description

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. 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, 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. Investigate failure modes, perform root cause analyses, and develop solutions to address technical challenges. Ensure compliance with relevant regulatory requirements and standards. 5. Performs troubleshooting on commercial 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. May train and/or provide work direction to technicians. 10. Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success. 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 0 - 2 Years with MS • Experience with medical device development with product sourced from contract manufacturers • Experience with Design Controls & Risk Management practices. Other Details: • Schedule: 08:00:AM - 04:30:PM • Work Setup: Onsite in Maple Grove, MN • Contract Length: 6 Months

Responsibilities

The R&D Engineer II will develop products, materials, processes, or equipment for projects of moderate complexity. They will participate in project teams, conduct engineering tests, and ensure compliance with regulatory requirements.