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Engineering Medical Device Jobs in Minnesota (NOW HIRING)

Actalent

Med Device Scientist II

Maple Grove, MN

$30 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Med Device Scientist II This Scientist II role supports the development and optimization of drug ... Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biomedical Engineering ...

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All JobsEngineering Medical Device JobsEngineering Medical Device Jobs in Minnesota

Engineering Medical Device information

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$20

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How much do engineering medical device jobs pay per hour?

As of Aug 16, 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 does an engineering medical device do?

An engineering medical device professional designs, develops, and tests medical equipment such as diagnostic tools, surgical instruments, and monitoring systems. They apply engineering principles, often using CAD software and regulatory standards, to ensure devices are safe, effective, and compliant with healthcare regulations.

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 82% Full Time, and 18% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $101,528 per year, or $48.8 per hour.

Senior Software Business Analyst - Medical Device (Hybrid - Maple Grove, MN) - Contract

Pharmavise

Maple Grove, MN • On-site

$94K - $122K/yr

Contractor

Re-posted 15 days ago

Job description


Our Fortune 500 Medical Device client has an exciting opportunity for a Senior Software Business Analyst.
Job Summary:
We are seeking an experienced Senior Software Business Analyst to join our dynamic team in the medical device industry. This role is critical to bridging the gap between clinical users, business stakeholders, and software development teams. The ideal candidate will possess strong analytical skills, in-depth knowledge of software development practices, and a deep understanding of regulatory and compliance requirements specific to healthcare and medical device software (e.g., FDA, ISO 13485, IEC 62304).
Responsibilities:
• Collaborate with cross-functional teams including product managers, engineers, QA, regulatory, and clinical experts to define software requirements for medical device products.
• Elicit, document, and manage business and functional requirements using industry-standard techniques (e.g., user stories, use cases, process flows).
• Translate complex clinical and business needs into detailed software requirements specifications (SRS).
• Act as the primary liaison between business stakeholders and development teams throughout the product lifecycle.
• Ensure software solutions align with regulatory standards and risk management processes (e.g., design control, traceability, usability).
• Support software validation and verification efforts by reviewing test plans and ensuring requirements coverage.
• Contribute to continuous improvement initiatives within the software development and requirements management processes.
• Facilitate requirement change management processes and impact analysis.
• Participate in audits and regulatory submissions as needed.
Qualifications:
• Bachelor's or Master's degree in Business, Engineering, Computer Science, Biomedical Engineering, or related field.
• 5+ years of experience as a Business Analyst, including at least 2 years in a senior or lead role.
• Proven experience in the medical device industry or regulated healthcare software environment.
• Strong knowledge of IEC 62304, ISO 13485, 21 CFR Part 11, and FDA Design Controls.
• Solid understanding of Agile, Scrum, and/or Waterfall methodologies.
• Proficiency with tools such as Jira, Confluence, Azure DevOps, and requirements management software such as Jama (highly preferred)
• Exceptional communication skills with the ability to convey technical concepts to non-technical stakeholders.
• Strong analytical mindset and attention to detail.
Preferred Qualifications
• Experience with SaMD (Software as a Medical Device) or embedded systems.
• Familiarity with HL7, FHIR, DICOM, or other healthcare interoperability standards.
• Certification such as CBAP, PMI-PBA, or similar is a plus.
Why Join Us?
Work with cutting-edge medical technologies that improve patient outcomes. Collaborate with world-class professionals in a mission-driven organization focused on innovation, compliance, and quality.
Other Details:
• Schedule: 08:00:AM - 04:30:PM CST
• Work Setup: Hybrid at Maple Grove, MN
• Contract Length: 6 Months
• Start Date:9/2/2025

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