Research And Development Engineer

REQ Solutions; Maple Grove (MN); On-site; USD 55,104 - 64,747; Full time

Job summary

A specialized solutions company located in Maple Grove is seeking a mid-senior level engineer for a contract position. The ideal candidate will have strong CAD/SolidWorks experience and a background in medical device development. Responsibilities include product development, engineering testing, and cross-department collaboration. This role offers a pay range of $40.00/hr - $47.00/hr for at least 12 months.

Qualifications

• 2 to 4 years of experience with a relevant degree.
• Molded component development preferred.
• Experience in medical device development is highly preferred.

Responsibilities

• Develop products and materials for projects of moderate complexity.
• Compile, analyze, and report operational data to establish performance standards.
• Design and coordinate standard engineering tests and experiments.
• Collaborate with various departments for project success.
• Prepare documentation to communicate results.

Skills

CAD/SolidWorks experience

Medical Device experience

Troubleshooting skills

Data analysis skills

Education

BS degree in Mechanical Engineering or Bioengineering

Tools

MS Office

Job description

This range is provided by REQ Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$40.00/hr - $47.00/hr

Duration: 12+ Months (Possible temp to hire)

Location: Maple Grove, MN 55311

Onsite Role

Responsibilities

• MUST have CAD/SolidWorks experience
• Develops products, materials, processes, or equipment for projects of moderate complexity.
• Compiles, analyzes, and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials.
• Fully participates in and successfully contributes to project teams typically including activities such as 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 the 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.

Education/Experience

• 2 - 4 Years with BS degree in ME or Bioengineering
• Molded component development preferred.
• Medical Device experience highly preferred
• MUST have CAD/SolidWorks experience
• MS Office

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Industries: Medical Equipment Manufacturing