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Medical Device Research Jobs in Minnesota (NOW HIRING)

Vantive

Senior Principal Quality Engineer

Oakdale, MN · On-site

Your Role The Senior Principal Quality Engineer is responsible for leading quality support and sustaining activities for Drug Products & Medical Device Research & Development activities related to ...

Vantive

Senior Principal Quality Engineer

Oakdale, MN · On-site

Your Role The Senior Principal Quality Engineer is responsible for leading quality support and sustaining activities for Drug Products & Medical Device Research & Development activities related to ...

Vantive

Senior Principal Quality Engineer

Oakdale, MN · On-site

$160K/yr

Your Role The Senior Principal Quality Engineer is responsible for leading quality support and sustaining activities for Drug Products & Medical Device Research & Development activities related to ...

Aerotek

Catheter Builder

Maple Grove, MN

R&D Medical Device Assembler Company Description We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with ...

Gateway Recruiting

Medical Director

Minneapolis, MN

This role will be the voice of the physician and patient and will partner with Clinical, Research ... Working knowledge of clinical trial methodology, Good Clinical Practice (GCP), medical device ...

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All JobsMedical Device Research JobsMedical Device Research Jobs in Minnesota

Medical Device Research information

See Minnesota salary details

$36.7K

$52.2K

$57.3K

How much do medical device research jobs pay per year?

As of Sep 3, 2026, the average yearly pay for medical device research in Minnesota is $52,228.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,900.00 and $56,800.00 per year, depending on experience, location, and employer.

What is medical device research?

Medical device research involves the development, testing, and evaluation of medical devices to ensure their safety, effectiveness, and regulatory compliance before they reach the market. This research covers a range of activities, including preclinical studies, clinical trials, and post-market surveillance. Professionals in this field work closely with engineers, healthcare providers, and regulatory bodies to develop innovations that improve patient care.

What are the key skills and qualifications needed to thrive in medical device research?

To excel in Medical Device Research, a strong background in biomedical engineering, life sciences, or a related field is essential, often accompanied by advanced degrees. Familiarity with regulatory standards (such as FDA or ISO), clinical trial management systems, and data analysis tools is highly valuable. Exceptional problem-solving, teamwork, and attention to detail help professionals innovate and navigate complex project requirements. These skills are crucial for ensuring rigorous research, regulatory compliance, and the successful development of safe and effective medical devices.

What are some typical challenges faced by professionals working in medical device research?

Professionals in Medical Device Research often encounter challenges such as navigating complex regulatory requirements, ensuring patient safety during clinical trials, and meeting strict documentation standards. Balancing innovation with compliance can be demanding, as teams must integrate new technologies while adhering to FDA or international regulations. Effective collaboration with cross-functional teams—including engineers, clinicians, and regulatory specialists—is essential to address these challenges and drive projects toward successful approval and market release.
Medical Device Research jobs near you
Infographic showing various Medical Device Research job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 15% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $52,228 per year, or $25.1 per hour.

Quality Engineer Medical Device

Egg Medical Inc

Roseville, MN • On-site

$100K - $115K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 17 days ago

Job description

Summary

We are seeking a Quality Engineer to add to our team! This position will support the management of our quality system while actively contributing to new product design and development initiatives. This role combines core quality engineering responsibilities with technical involvement in engineering projects to ensure our innovative medical devices meet the highest standards of safety, reliability, and regulatory compliance. 

Key Responsibilities

  • Quality System Support: Develop, implement, and maintain elements of the Quality Management System (QMS) to ensure ongoing compliance with FDA regulations, ISO 13485, and other applicable standards.
  • New Product Development & Design Control: Collaborate with R&D, engineering, and cross-functional teams on new design projects; support design inputs/outputs, risk assessments (e.g., FMEA, ISO 14971), design verification and validation activities, and design reviews/transfer to manufacturing.
  • Risk Management & Technical Reviews: Perform and document risk analyses, participate in technical design reviews, and ensure design controls are effectively applied throughout the product lifecycle.
  • Non-Conformance & Corrective Actions: Investigate non-conformances, lead root cause analysis, and implement corrective and preventive actions (CAPA) to drive continuous improvement and prevent recurrence.
  • Documentation & Compliance: Maintain accurate quality records, support internal/external audits, and contribute to regulatory submissions as needed.
  • Continuous Improvement: Identify opportunities to improve quality processes, product designs, and overall efficiency; partner with engineering and other teams on quality initiatives

Qualifications

  • Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Quality Engineering, or a related field.
  • 3+ years of experience as a Quality Engineer in a regulated industry, preferably medical devices.
  • Experience with FDA regulations, ISO 13485, and other medical device quality standards.
  • Proficiency in quality tools and methodologies (e.g., FMEA, SPC, CAPA).

Compensation & Benefits

  • Full-time position with salary range from $100,000-$115,000, depending on experience.
  • Additional bonus/incentive compensation available.
  • Company laptop provided.
  • Insurance available on the 1st of the month following date of hire, including: health, dental and vision insurance, plus pre-tax or Roth 401k available after 30 days.
  • PTO accrues starting at 15 days, plus 11 company paid holidays.

Company Description

Egg Medical is an innovative leader in radiation safety protection technology. Our mission is to protect healthcare professionals from occupational radiation exposure while enabling the delivery of exceptional patient care.