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Quality Engineer Medical Devices Jobs in Michigan

Quality Engineer

Clinton, MI · On-site

$71K - $91K/yr

Acts as the primary advocate for compliance and Quality Assurance Engineering of medical devices and medical device components for the development of Validation programs and program compliance ...

Quality Engineer

Romulus, MI

$69K - $89K/yr

Our company is seeking a skilled Quality Engineer to join our team. We are a Tier II automotive supplier. Following are the job duties: - Conduct quality inspections and analyze product ...

QUALITY ENGINEER

Ferndale, MI · On-site

$67K - $86K/yr

Proficiency using handheld inspection equipment and surface plate measurement devices. * Ability to ... Certified Quality Engineer (CQE) * Internal Auditor Certification * Lean Six Sigma Certification

Quality Engineer

Lapeer, MI

$66K - $85K/yr

The Quality Engineer supports new product/process development and manufacturing through the ... Determines the methods/devices that will be used for inspection * Collaborates with Manufacturing ...

Quality Engineer

Lapeer, MI · On-site

$66K - $85K/yr

The Quality Engineer supports new product/process development and manufacturing through the ... Determines the methods/devices that will be used for inspection * Collaborates with Manufacturing ...

Quality Engineer

Novi, MI · On-site

$67K - $87K/yr

Founded as EJ Brooks & Company, Brooks grew to incorporate Meter Devices Company and Ekstrom ... The Quality Engineer is a key driver of continuous improvement, product reliability, and customer ...

Quality Engineer

Freeland, MI · On-site

$70K - $80K/yr

... devices, and advanced power solutions for the aerospace, defense, and medical industries. They are hiring a Quality Engineer at their facility in Freeland, MI. This is a Permanent position with our ...

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Quality Engineer

Southfield, MI · On-site

$85K - $110K/yr

Quality Engineer Quality Engineer has overall responsibility to ensure new products are launched with adequate controls in place. They will establish product quality controls , process controls , and ...

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Quality Engineer

Warren, MI · On-site

$85K - $110K/yr

Quality Engineer Quality Engineer has overall responsibility to ensure new products are launched with adequate controls in place. They will establish product quality controls , process controls , and ...

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Quality Engineer

Sterling Heights, MI · On-site

$85K - $110K/yr

Quality Engineer Quality Engineer has overall responsibility to ensure new products are launched with adequate controls in place. They will establish product quality controls , process controls , and ...

Medical, Dental, HSA Contribution, 401(k), PTO Location: Grand Haven, MI | Onsite Overview of the Quality Engineer Position: The Quality Engineer is responsible for driving product and process ...

Quality Engineer

Clinton Township, MI · On-site

$66K - $86K/yr

Acts as the primary advocate for compliance and Quality Assurance Engineering of medical devices and medical device components for the development of Validation programs and program compliance ...

Quality Engineer

Clinton Township, MI · On-site

$66K - $86K/yr

Acts as the primary advocate for compliance and Quality Assurance Engineering of medical devices and medical device components for the development of Validation programs and program compliance ...

Sr. Quality Engineer

Lapeer, MI

$81K - $110K/yr

The Quality Engineer supports new product/process development and manufacturing through the ... Determines the methods/devices that will be used for inspection * Collaborates with Manufacturing ...

Quality Engineer

Manchester, MI

$66K - $85K/yr

As a Quality Engineer, you will play a key role in ensuring that our products meet the highest standards of quality and reliability. Responsibilities: * Collaborate with cross-functional teams to ...

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Showing results 1-20

Quality Engineer Medical Devices information

See Michigan salary details

$39.2K

$73.2K

$103.7K

How much do quality engineer medical devices jobs pay per year?

As of Aug 12, 2026, the average yearly pay for quality engineer medical devices in Michigan is $73,248.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,800.00 and $81,100.00 per year, depending on experience, location, and employer.

What does a quality engineer do in the medical device industry?

A Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory standards and quality requirements throughout their lifecycle. They develop and implement quality control processes, conduct risk assessments, lead investigations into product defects, and work closely with cross-functional teams to ensure compliance with regulations such as FDA and ISO 13485. Their work helps to guarantee the safety, reliability, and effectiveness of medical devices before they reach patients.

How does a quality engineer collaborate with cross-functional teams in the medical device industry?

Quality Engineers in the medical device field work closely with design, manufacturing, and regulatory teams to ensure products meet stringent quality and compliance standards. They participate in design reviews, help develop verification and validation protocols, and support the implementation of corrective actions. Regular communication with production and R&D teams is essential to identify potential risks early and to ensure that quality is built into every stage of product development. This collaborative approach not only improves product safety and efficacy but also streamlines regulatory submissions and audits.

What is the difference between Quality Engineer Medical Devices vs Quality Technician Medical Devices?

AspectQuality Engineer Medical DevicesQuality Technician Medical Devices
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, basic quality certifications
ResponsibilitiesDesigning quality systems, process improvements, root cause analysisInspecting products, conducting tests, recording quality data
Work EnvironmentDesign and development labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsageMedical device companies, OEMs, suppliersManufacturers, contract labs, quality departments

In summary, Quality Engineer Medical Devices focus on developing quality systems, process improvements, and ensuring compliance, while Quality Technicians primarily perform product inspections and testing. Both roles are essential in maintaining high standards in the medical device industry but differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a quality engineer in medical devices, and why are they important?

To thrive as a Quality Engineer in Medical Devices, you typically need a degree in engineering or a related field, combined with knowledge of quality assurance principles and regulatory requirements (such as ISO 13485 and FDA regulations). Familiarity with risk management tools, validation protocols, and quality management systems (QMS), as well as certifications like CQE (Certified Quality Engineer), are highly valuable. Strong analytical thinking, attention to detail, and effective communication skills enable you to identify issues, collaborate with cross-functional teams, and ensure compliance. These competencies are crucial for maintaining product safety, meeting regulatory standards, and supporting a culture of continuous improvement in the medical device industry.
What are popular job titles related to Quality Engineer Medical Devices jobs in Michigan? For Quality Engineer Medical Devices jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Quality Engineer Medical Devices jobs in Michigan look for? The top searched job categories for Quality Engineer Medical Devices jobs in Michigan are:
What cities in Michigan are hiring for Quality Engineer Medical Devices jobs? Cities in Michigan with the most Quality Engineer Medical Devices job openings:
Infographic showing various Quality Engineer Medical Devices job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 1% Temporary, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $73,248 per year, or $35.2 per hour.

$85K - $115K/yr

Full-time

Re-posted 25 days ago


Job description

We are looking to hire an experienced Senior Quality Engineer II. As the Senior Quality Engineer II, you will identify, analyze, critique, and correct quality control processes and documented procedures. In this role, you will also interact with a variety of suppliers and the Genesis family of companies to ensure consistency, accuracy, and the implementation of best practices.


Genesis Innovation Group (GIG) is a unique Venture Capital and Business Development firm concentrated on medical devices. Our role as investors and industry partners is to focus on the creative power of entrepreneurs by leveraging our network, resources, and experience to ensure their success. Combined, we have more than a century of experience in the medical device space, and over two hundred patents and innovations to our names.


In this role you will:

  • Formulate or help formulate quality assurance policies and procedures
  • Review and provide input to design plans, user requirements, design inputs, test procedures, risk management file, and design outputs to understand the scope, requirements, and function of the systems
  • Ensure that products meet the organizations and customers' quality and product integrity requirements
  • Support the product development team by providing analysis and expertise throughout the inspection process
  • Identify root causes of problems in the production process; recommend and/or implements corrective measures
  • Analyze data to identify trends in product quality or defects with a goal of mitigating and preventing recurrence and future defects
  • Ensure manufacturing processes comply with federal, state, local, and industry standards and regulations
  • Perform risk analysis as part of the risk management team
  • Perform gap analyses on standards and regulations as new customers are brought onboard and as new or revised standards are released
  • Conduct training on quality assurance concepts and tools
  • Monitor, manage and handle complaints, feedback, and non-conforming products
  • Find, devise, handle, and enforce corrective and preventative actions
  • Communicate with engineering and productions within an organization and with customers and suppliers on quality-related issues
  • Work within the QMS team to ensure the overall quality of a manufactured product.
  • Create, support, and oversee documentation
  • Develop quality control systems
  • Analyze quality assurance test results to ensure that the end product meets the exact needs of the user

Tokeep up with our fast-paced, detail-driven business qualified candidates will have:

  • Bachelor of Science in Engineering or related degree required
  • Specific Medical quality design experience required
  • Minimum of 6 years of related experience in a regulated environment
  • Experience in the medical device industry preferred
  • Experience with Design Controls and Risk Management required
  • Experience with complaint and CAPA handling a plus
  • Geometric Dimensioning and Tolerancing experience a plus
  • Ability to work individually and on a team
  • Ability to solve quality issues with remote suppliers
  • High attention to detail


Why Join Genesis Innovation Group:


If you are looking to further your career in a pioneering and evolving industry, consider joining our team of professionals. We value and appreciate our employees and will support you with great company culture and opportunities for professional growth. At Genesis Innovation Group, we provide competitive wages, a bonus program, benefits, and strong team collaboration. Apply today for immediate and confidential consideration to become our next Senior Quality Engineer II. To learn more about us, visit us online at www.genesisinnovationgroup.com.