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Contract Quality Engineer Medical Device Jobs in Michigan

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Support buildout of a Quality Management System (QMS) in anticipation of future ISO 13485 ... Experience working alongside a contract manufacturer or external build partner on clinical or early ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

... engineering drawings, work instructions, and quality standards * Inspect finished assemblies for ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Staff Advanced Quality Engineer Portage, MI Join a team focused on advancing quality throughout the product development lifecycle in a regulated medical device environment. As a Staff Advanced ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

... engineering drawings, work instructions, and quality standards * Inspect finished assemblies for ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

... engineering drawings, work instructions, and quality standards * Inspect finished assemblies for ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Hybrid Staff Advanced Quality Engineer Portage, MI Join a team focused on advancing quality throughout the product development lifecycle in a regulated medical device environment. As a Staff Advanced ...

Hybrid Staff Advanced Quality Engineer Portage, MI Join a team focused on advancing quality throughout the product development lifecycle in a regulated medical device environment. As a Staff Advanced ...

Quality Engineer

Kingsford, MI

$66K - $85K/yr

Identifies unique contract quality requirements and assures they are flowed down to supply chain ... We offer a comprehensive benefits package that includes competitive medical, dental, and vision ...

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 ...

As the Quality Engineer - Service , you will join a team that supports the quality, reliability ... Experience in medical device development, manufacturing, servicing, or another regulated industry ...

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

Experience supporting complex assemblies, precision components, optics, semiconductor, medical device, aerospace, or other high-technology manufacturing environments. * ASQ Certified Quality Engineer ...

Experience supporting complex assemblies, precision components, optics, semiconductor, medical device, aerospace, or other high-technology manufacturing environments. * ASQ Certified Quality Engineer ...

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Experience supporting complex assemblies, precision components, optics, semiconductor, medical device, aerospace, or other high-technology manufacturing environments. * ASQ Certified Quality Engineer ...

Experience supporting complex assemblies, precision components, optics, semiconductor, medical device, aerospace, or other high-technology manufacturing environments. * ASQ Certified Quality Engineer ...

Sr. Quality Engineer

Marquette, MI · On-site

$69K - $90K/yr

Quality Engineer - Quality Control (QC QE)Position Summary The Quality Engineer - Quality Control ... Medical device or other regulated manufacturing experience preferred. * Knowledge of ISO 13485 and ...

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Contract Quality Engineer Medical Device information

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

A Contract Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory and company quality standards during a specific project or timeframe. They typically work on a contract basis, focusing on tasks like process validation, risk management, root cause analysis, and compliance with standards such as ISO 13485 and FDA regulations. Their role often involves collaborating with engineering, production, and regulatory teams to troubleshoot quality issues and implement corrective actions. They play a key role in maintaining product safety and regulatory compliance throughout the manufacturing process.

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

To thrive as a Contract Quality Engineer in the Medical Device field, you need expertise in quality assurance, regulatory compliance (such as ISO 13485 and FDA regulations), and a background in engineering or life sciences. Familiarity with tools like CAPA systems, risk management software, and proficiency in quality management systems (QMS) is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These skills are essential to ensure product safety, regulatory compliance, and the successful launch and maintenance of medical devices in a highly regulated environment.

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

As a Contract Quality Engineer in the medical device sector, you will frequently work closely with cross-functional teams, including R&D, manufacturing, regulatory affairs, and supply chain. Your responsibilities often involve reviewing design documentation, participating in risk assessments, and ensuring production processes meet both internal quality standards and regulatory requirements. Effective communication is key, as you'll be responsible for conveying quality expectations, addressing non-conformities, and supporting project timelines. This collaborative environment provides valuable experience in coordinating with diverse professionals while upholding strict industry standards.

What is the difference between Contract Quality Engineer Medical Device vs Contract Quality Engineer Pharmaceutical?

AspectContract Quality Engineer Medical DeviceContract Quality Engineer Pharmaceutical
CertificationsISO 13485, FDA QSR, GMPICH Q7, GMP, FDA regulations
Work EnvironmentMedical device manufacturing, labs, compliance auditsPharmaceutical production, labs, quality assurance
Industry UsageMedical device companies, OEMs, suppliersPharmaceutical firms, biotech companies, contract manufacturers

Both roles focus on quality assurance and regulatory compliance but differ mainly in industry-specific standards and environments. Contract Quality Engineers Medical Device work primarily with ISO 13485 and FDA QSR standards in device manufacturing, while Contract Quality Engineers Pharmaceutical focus on GMP and ICH Q7 regulations in drug production. Understanding these differences helps candidates target the right industry and certifications for their career goals.

What are the most commonly searched types of Quality Engineer Medical Device jobs in Michigan?

The most popular types of Quality Engineer Medical Device jobs in Michigan are:

What are popular job titles related to Contract Quality Engineer Medical Device jobs in Michigan?

For Contract Quality Engineer Medical Device jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Contract Quality Engineer Medical Device jobs in Michigan look for?

The top searched job categories for Contract Quality Engineer Medical Device jobs in Michigan are:

What cities in Michigan are hiring for Contract Quality Engineer Medical Device jobs?

Cities in Michigan with the most Contract Quality Engineer Medical Device job openings:

Systems Engineer - Medical Device Company

Mitovation

Ann Arbor, MI • On-site

$110K - $140K/yr

Full-time

Medical

Posted 17 days ago

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Job description

About Mitovation

Mitovation is a clinical-stage medical device company developing a near-infrared photobiomodulation (NIR-PBM) therapy that protects the brain from reperfusion injury after cardiac arrest. The technology originated from mitochondrial biology research at Wayne State University and the University of Michigan and has progressed through an active FDA Investigational Device Exemption (IDE) and a pediatric clinical study. This position is funded through Mitovation's NIH Cooperative Agreement grant.

Position Summary

The Systems Engineer will be one of the first engineering hires at Mitovation, helping stand up a new company office in the Ann Arbor/Detroit, MI area. This role owns system-level architecture, integration, and verification across hardware, firmware, optics, and software subsystems, and works directly with Mitovation's external manufacturing partners to assist with the build of the clinical study systems used at trial sites.

Key Responsibilities

Clinical system support:

•      Own system-level builds and testing for the clinical study device platform, working with our manufacturing partner.

•      Support IDE maintenance and contribute engineering documentation supporting the clinical study.

New system design / development:

•      Translate clinical and user needs into system, subsystem, and component-level technical requirements, and maintain traceability through the design history file.

•      Lead system integration across electrical, mechanical, optical, firmware, and software subsystems, coordinating with the manufacturing partner throughout the build process.

•      Develop and execute verification and validation (V&V) test protocols; author associated technical reports.

•      Support risk management activities (FMEA, hazard analysis) in accordance with ISO 14971 and Class II medical device design controls.

•      Help stand up engineering processes and documentation at the new company office as an early technical hire.

•      Support buildout of a Quality Management System (QMS) in anticipation of future ISO 13485 certification.

Required Qualifications

•      Bachelor's degree in Biomedical, Electrical, Mechanical, or Systems Engineering (or related field); advanced degree a plus.

•      5+ years of systems engineering experience in medical devices, with direct experience in design controls (21 CFR 820.30 / ISO 13485).

•      Demonstrated experience taking a device from prototype/early clinical stage through design V&V.

•      Working knowledge of risk management standards (ISO 14971) and IEC 60601 electrical safety requirements for medical electrical equipment.

•      Comfort working in a small-company, early-stage environment — willing to be hands-on with builds and testing as well as documentation and process.

•      Strong cross-functional communication skills; able to work directly with founders, clinical partners, and the external manufacturing partner.

Preferred Qualifications

•      Experience with optical or light-based therapeutic devices (photobiomodulation, phototherapy, laser/LED systems).

•      Experience working alongside a contract manufacturer or external build partner on clinical or early-production device units.

•      Familiarity with FDA IDE and De Novo/510(k) regulatory pathways.

What Mitovation Offers

•      The opportunity to build the engineering foundation of a company developing a first-in-category neuroprotection therapy, with FDA IDE already in hand and an active clinical study underway.

•      A seat at the table during a pivotal growth phase — this hire directly shapes the technical team and the new company office.

•      Competitive salary and benefits, commensurate with an early-stage medical device company.

Company Description

Mitovation is a Michigan based medical device startup company with their first product treating post cardiac arrest re-perfusion injury.
Why is this a breakthrough? Cardiac arrest impairs systemic perfusion and renders the brain and other organs ischemic. The brain is highly reliant on a constant supply of oxygen and nutrients and thus is particularly sensitive to the resultant deficit in blood flow. In the absence of rapid resuscitation and restoration of blood flow, ischemia leads to severe neurologic damage. While resuscitation is required to preserve neurologic function, it also initiates re-perfusion injury, which plays a major role in the compromised recovery of resuscitated patients, and is thought to contribute significantly to the high incidence of morbidity and mortality associated with cardiac arrest. Despite advances in cardiopulmonary resuscitation, neurological function – a primary metric for clinical outcome – remains poor following cardiac arrest and resuscitation.

Mitovation has developed a breakthrough technology to prevent the brain damage that occurs from a cardiac arrest.