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Engineering Medical Device Jobs in Minnesota (NOW HIRING)

Medtronic

Engineering Manager

Fridley, MN · On-site

Medical device industry experience supporting released products or sustaining engineering organizations. * Experience with corrective and preventive action (CAPA), complaint investigations, risk ...

Medtronic

Engineering Manager

Fridley, MN · On-site

Medical device industry experience supporting released products or sustaining engineering organizations. * Experience with corrective and preventive action (CAPA), complaint investigations, risk ...

BEPC INC

Operator I_MN ONLY - 30467_M

Saint Paul, MN · On-site

$17.75 - $18.75/hr

Medical Device Assembler Location: Saint Paul, MN (55112) Employment Type: W2 Contract - 6 Months ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

BEPC INC

Be Seen First

Operator I_MN ONLY - 30467_M

Saint Paul, MN · On-site

$17.75 - $18.75/hr

Medical Device Assembler Location: Saint Paul, MN (55112) Employment Type: W2 Contract - 6 Months ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

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All JobsEngineering Medical Device JobsEngineering Medical Device Jobs in Minnesota

Engineering Medical Device information

See Minnesota salary details

$20

$48

$94

How much do engineering medical device jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for engineering medical device in Minnesota is $48.81, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $58.37 per hour, depending on experience, location, and employer.

What is an engineering medical device professional?

Engineering medical device professionals are specialists who design, develop, test, and improve medical devices used in healthcare. They combine principles of engineering, biology, and medicine to create equipment such as pacemakers, imaging machines, and prosthetics that help diagnose, treat, or manage medical conditions. Their work ensures devices are safe, effective, and comply with regulatory standards. These professionals often work closely with doctors, patients, and regulatory agencies throughout the product development process.

What are the key skills and qualifications needed to thrive as a medical device engineer?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant degree and knowledge of FDA regulations. Familiarity with CAD software, prototyping tools, and quality management systems is typically required, along with certifications like Six Sigma or ISO 13485. Strong problem-solving abilities, teamwork, and effective communication are standout soft skills in this role. These competencies are crucial for designing safe, innovative devices that meet regulatory standards and improve patient outcomes.

What are some typical challenges faced by engineers working in the medical device industry?

Engineers in the medical device industry often face challenges related to strict regulatory compliance, such as meeting FDA or ISO standards. Additionally, they must ensure that devices are safe, effective, and user-friendly, requiring frequent collaboration with cross-functional teams like clinical, quality assurance, and manufacturing. Balancing innovation with patient safety while managing tight project timelines is also a common aspect of the role. Overcoming these challenges can be rewarding, as it directly contributes to improving patient outcomes.

What is the difference between Engineering Medical Device vs Biomedical Engineer?

AspectEngineering Medical DeviceBiomedical Engineer
Required CredentialsEngineering degree, possibly certifications in medical device designEngineering or biomedical degree, certifications in healthcare technology
Work EnvironmentDesign labs, manufacturing facilities, regulatory agenciesHospitals, research labs, healthcare companies
Employer & Industry UsageMedical device companies, biotech firms, regulatory bodiesHospitals, medical research institutions, healthcare technology firms

Engineering Medical Device professionals focus on designing, developing, and testing medical devices, often working in manufacturing or regulatory settings. Biomedical Engineers have a broader scope, integrating engineering principles with biological sciences to improve healthcare solutions, including medical devices. While both roles require engineering backgrounds, Engineering Medical Device specialists typically concentrate on product development, whereas Biomedical Engineers may work on research, clinical applications, or device integration.

What are the most commonly searched types of Engineering Medical Device jobs in Minnesota?

The most popular types of Engineering Medical Device jobs in Minnesota are:

What are popular job titles related to Engineering Medical Device jobs in Minnesota?

For Engineering Medical Device jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Engineering Medical Device jobs in Minnesota look for?

The top searched job categories for Engineering Medical Device jobs in Minnesota are:

What cities in Minnesota are hiring for Engineering Medical Device jobs?

Cities in Minnesota with the most Engineering Medical Device job openings:

Engineering Medical Device jobs near you
Infographic showing various Engineering Medical Device job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 11% Part Time, and 9% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $101,528 per year, or $48.8 per hour.

Quality Engineer - Medical Devices

Stark Pharma Solutions Inc

Minneapolis, MN • On-site

$75K - $97K/yr

Contractor

Re-posted 18 days ago

Job description

Job Title: Quality Assurance Engineer – Medical Devices

Location: Northwest Minneapolis Metro Area

Type: 6-Month Contract-to-Hire

Job Summary

Seeking a Quality Assurance Engineer to support quality systems, manufacturing operations, CAPA, validation, audits, and DHF activities within a medical device environment. This role will partner cross-functionally to ensure compliance with FDA and ISO standards throughout the product lifecycle.

Key Responsibilities

  • Manage CAPAs, nonconformances, root cause investigations, and change controls
  • Support IQ/OQ/PQ validation activities and review quality documentation
  • Maintain DHF documentation and support product lifecycle activities
  • Review batch records, work orders, and manufacturing documentation for GMP compliance
  • Support incoming inspection, supplier quality, and audit readiness
  • Analyze quality metrics and drive continuous improvement initiatives
  • Support customer complaint investigations and PLM system updates

Required Qualifications

  • Bachelor’s degree in Engineering, Life Sciences, or related field
  • 5+ years of medical device quality or design assurance experience
  • Strong knowledge of FDA 21 CFR 820, ISO 13485, and ISO 14971
  • Experience with CAPA, NCs, DHF, audits, and validation activities
  • Familiarity with PLM systems such as Windchill, Agile, or Propel