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Quality Engineer Medical Devices Jobs in Michigan

Quality Engineer, Service

Kalamazoo, MI · On-site

$69K - $110K/yr

As the Quality Engineer - Service , you will join a team that supports the quality, reliability, and serviceability of medical devices throughout their lifecycle. This role partners closely with ...

Quality Engineer, Service

Kalamazoo, MI · On-site

$69K - $110K/yr

As the Quality Engineer - Service , you will join a team that supports the quality, reliability, and serviceability of medical devices throughout their lifecycle. This role partners closely with ...

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

Lapeer, MI · On-site

$70 - $110/hr

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 ...

New

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

Novi, MI · On-site

$80 - $110/hr

Quality Engineer Brooks Utility Products Novi, Michigan, United States About this position Brooks ... Brooks & Company, Meter Devices Company, and Ekstrom Industries into the industry's most ...

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

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

Brooks & Company, Meter Devices Company, and Ekstrom Industries into the industry's most ... The Quality Engineer is a key driver of continuous improvement, product reliability, and customer ...

Quality Engineer

Novi, MI · On-site

$67K - $87K/yr

Brooks & Company, Meter Devices Company, and Ekstrom Industries into the industry's most ... 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

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 ...

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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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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 29, 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 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 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 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, 73% Full Time, 16% Part Time, 2% Temporary, 7% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $73,248 per year, or $35.2 per hour.

Quality Engineer, Service

Stryker

Kalamazoo, MI • On-site

$69K - $110K/yr

Full-time

Posted 16 days ago


Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

130th of 495 rated machine equipment manufacturers


Job description

Work Flexibility: Onsite

Stryker is hiring a Quality Engineer - Service to join our Instruments division. This is an onsite position based in Kalamazoo, MI.

As the Quality Engineer - Service, you will join a team that supports the quality, reliability, and serviceability of medical devices throughout their lifecycle. This role partners closely with service, engineering, and operations teams to ensure products, processes, and repair activities meet quality and regulatory requirements while minimizing customer disruption. You will contribute to quality investigations, risk assessments, process improvements, and validation activities that support service operations across multiple functions.

What You Will Do

  • Support quality activities for depot service, field service, loaner, refurbishment, and device service operations, including validation and nonconformance management.

  • Conduct risk assessments on product and process nonconformances to evaluate potential patient and user impact and define appropriate corrective actions.

  • Review, investigate, and document product nonconformances in a timely manner to support efficient product disposition and reduce customer downtime.

  • Partner with engineering teams to resolve service-related product issues and support continuity of operations.

  • Support product and process validation activities, including qualification of new equipment, fixtures, and service-related processes.

  • Develop, revise, and maintain quality procedures, inspection methods, and documentation to ensure compliance with regulatory and quality system requirements.

  • Analyze operational, complaint, and customer feedback data and prepare reports and presentations to support quality reviews and decision-making.

  • Participate in cross-functional improvement initiatives, internal audits, and quality investigations to identify and implement process enhancements.

What You Need

Required

  • Bachelor's degree in Engineering or a related technical discipline

  • 0+ years' experience in engineering

Preferred

  • Experience in medical device development, manufacturing, servicing, or another regulated industry environment

  • Knowledge of FDA regulations, ISO standards, and applicable quality system requirements

  • Knowledge of risk analysis, root cause analysis, statistical methods, and quality investigation techniques

  • ASQ certification, including Certified Quality Engineer (CQE), Certified Reliability Engineer (CRE), Certified Manager of Quality/Organizational Excellence (CMQ/OE), or Certified Six Sigma Black Belt (CSSBB)

  • USN: $69,500 - $110,900 USD Annual
Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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