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Medical Device Consulting Jobs in Michigan (NOW HIRING)

Omnex Inc

Omnex Consultant ISO 13485

Ann Arbor, MI · On-site

$80 - $100/hr

... consulting, training and software development company (www.omnex.com) based in Ann Arbor, MI, has significant opportunities for highly qualified consultants to help with efforts in the Medical Device ...

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Stark Pharma Solutions Inc

Technician

Portage, MI · On-site

About the Company Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA ...

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MMS

Senior Medical Writer (Remote)

Canton, MI · On-site

... device industries with a proven, scientific approach to complex trial data and regulatory ... Take ownership of a given assignment, proactively consulting other project team members and other ...

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All JobsMedical Device Consulting JobsMedical Device Consulting Jobs in Michigan

Medical Device Consulting information

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$18

$43

$84

How much do medical device consulting jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for medical device consulting in Michigan is $43.44, according to ZipRecruiter salary data. Most workers in this role earn between $30.58 and $51.97 per hour, depending on experience, location, and employer.

What does a medical device consultant do?

A Medical Device Consultant provides expertise to companies developing, manufacturing, or marketing medical devices. They help navigate regulatory requirements, ensure compliance with FDA or EU MDR guidelines, conduct quality assessments, and offer strategic advice on product development. Consultants may also assist with clinical trials, risk management, and market entry strategies. Their goal is to help companies bring safe and effective medical devices to market efficiently while meeting industry regulations.

What are some typical daily responsibilities for professionals in medical device consulting?

Day-to-day tasks for Medical Device Consultants often include advising clients on regulatory strategy, preparing submissions for compliance agencies, assessing product safety and efficacy data, and coordinating with cross-functional teams such as R&D, quality assurance, and marketing. You may also conduct audits, lead training sessions, and assist clients in navigating clinical trial requirements or post-market surveillance. Collaboration and regular communication with client stakeholders are essential, as is staying current on evolving industry standards. This dynamic role provides exposure to diverse projects and the opportunity to make a tangible impact on the development and approval of innovative medical technologies.

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

To thrive in Medical Device Consulting, you need a strong background in biomedical engineering, regulatory knowledge, and experience with product development or commercialization, often supplemented by a relevant degree and industry certifications. Expertise with FDA regulations, ISO standards, clinical trial management systems, and common project management tools is highly valued. Exceptional problem-solving, client communication, and adaptability are crucial soft skills for success. These competencies are vital to effectively guide clients through compliance, market entry, and product lifecycle challenges in a complex, high-stakes industry.

How to become a medical device consultant?

To become a medical device consultant, individuals typically need a background in biomedical engineering, healthcare, or related fields, along with experience in medical device development, regulatory compliance, or quality assurance. Earning certifications such as ISO 13485 Lead Auditor or Regulatory Affairs Certification can enhance credibility, and strong project management and communication skills are essential for success in this role.

What job categories do people searching Medical Device Consulting jobs in Michigan look for?

The top searched job categories for Medical Device Consulting jobs in Michigan are:

What cities in Michigan are hiring for Medical Device Consulting jobs?

Cities in Michigan with the most Medical Device Consulting job openings:

Medical Device Consulting jobs near you
Infographic showing various Medical Device Consulting job openings in Michigan as of August 2026, with employment types broken down into 62% Full Time, 25% Part Time, and 13% Contract. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $90,351 per year, or $43.4 per hour.

Electrical Compliance Engineer - Medical Device (IEC/ISO 60601, EMC, V&V)

Stark Pharma Solutions Inc

Michigan Center, MI • On-site

Contractor

Posted 4 days ago

Job description

Job Description:

ABOUT COMPANY:

Stark Pharma Solutions Inc is a life sciences staffing and consulting firm supporting pharmaceutical, biotechnology and medical device organizations across the United States. We place quality, validation, manufacturing and regulatory professionals with companies building and scaling FDA-regulated operations. Our clients range from established manufacturers to early-stage sites standing up their first quality systems.

Electrical Compliance Engineer – Medical Device (IEC/ISO 60601, EMC, V&V)

JOB SUMMARY:

Our client, a medical device manufacturer, is seeking an Electrical Compliance Engineer to support a third-generation medical device currently undergoing UL certification and verification testing. This role focuses on electrical product safety, V&V, EMC, and regulatory compliance activities, with immediate priority on final testing execution, documentation, and certification reporting under IEC/ISO 60601 (3rd Edition). The consultant will also provide compliance and regulatory input for an early-stage second-generation product program.
This is a hands-on product-safety testing role. Candidates whose background is limited to general quality/documentation work, without direct UL/CSA test-lab or hands-on 60601 testing experience, will not be a fit.

RESPONSIBILITIES:

  • Define and implement product safety program plans for complex device development programs
  • Create product safety test plans and ensure they meet third-party certifier requirements
  • Support lab personnel on compliance testing, design conformance, and product safety issues
  • Interface with Nationally Recognized Test Labs (NRTLs) and external bodies to achieve product certification
  • Apply design controls, change controls, and risk management per the Quality Management System
  • Partner within design teams to drive product safety, compliance, and industry best practices
  • Mentor and support early-career engineers in the product safety discipline as needed

QUALIFICATIONS:

  • Hands-on IEC/ISO 60601 (3rd Edition) testing experience
  • Strong electrical product safety testing background
  • Verification & Validation (V&V) experience
  • EMC testing and compliance experience
  • Direct experience supporting UL and/or CSA certification activities
  • Former UL or CSA test engineer, or Product Safety Engineer background, strongly preferred
  • Regulatory affairs and compliance experience specific to medical devices
  • Experience with both testing execution and regulatory strategy
  • Prior work in an accredited test lab environment (UL, CSA, or similar)
  • 5–10 years of relevant experience (targeting 7–8 years)
  • Must be legally authorized to work in the United States 
  • W2 employment only

HOW TO APPLY:

Please send your resume to deepika.b@starkpharma.com. In your email, please include your current location, your hourly rate expectation on W2, and your availability to start.