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Quality Engineer Medical Device Jobs in Michigan

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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 ...

Hybrid Join Stryker's Emergency Care business as an Associate Manager, Quality Engineering in ... S. and international medical device regulations and standards, including 21 CFR Part 820, ISO 13485 ...

Hybrid Join Stryker's Emergency Care business as an Associate Manager, Quality Engineering in ... S. and international medical device regulations and standards, including 21 CFR Part 820, ISO 13485 ...

Medical Assembler

Dexter, MI · On-site

$17.25 - $21/hr

Medical Device Manufacturing Company Duration: 12-Month Contract Location: Dexter, MI 48130 Shift ... Perform continuity checks, basic testing, and quality inspections. * Rework, modify, disassemble ...

Medical Assembler

Dexter, MI · On-site

$17.25 - $21/hr

Medical Device Manufacturing Company Duration: 12-Month Contract Location: Dexter, MI 48130 Shift ... Perform continuity checks, basic testing, and quality inspections. * Rework, modify, disassemble ...

Medical Assembler

Dexter, MI · On-site

$18 - $22/hr

Medical Device Manufacturing Company Duration: 12-Month Contract Location: Dexter, MI 48130 Shift ... Perform continuity checks, basic testing, and quality inspections. * Rework, modify, disassemble ...

Quality Engineer

Ann Arbor, MI · On-site

$75 - $110/hr

JOB SUMMARY The Quality Engineer is responsible for planning, coordinating, and completing broadly ... medical, industrial and communications industries. Through proven experience and innovation ...

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 ...

Quality Engineer

Auburn Hills, MI · On-site

$68K - $88K/yr

The Quality Engineer is responsible for supporting product and process quality across Engineering, Manufacturing, Test, Supply Chain, and Program execution at Technical Directions Inc. This role ...

Quality Engineer

Ann Arbor, MI · On-site

$70K - $91K/yr

The Quality Engineer is responsible for planning, coordinating, and completing broadly defined quality engineering assignments and small projects that support product and process quality, compliance ...

Quality Engineer

Ann Arbor, MI · On-site

$80 - $110/hr

JOB SUMMARY The Quality Engineer is responsible for planning, coordinating, and completing broadly ... medical, industrial and communications industries. Through proven experience and innovation ...

Quality Engineer

Livonia, MI · On-site

$65 - $95/hr

Roush Title Quality Engineer Location Livonia, MI Category Engineering & Design Hiring Type ... Knowledge of manufacturing engineering skills Our full-time benefits include: medical, dental ...

Quality Engineer

Ann Arbor, MI · On-site

$70K - $91K/yr

The Quality Engineer is responsible for planning, coordinating, and completing broadly defined quality engineering assignments and small projects that support product and process quality, compliance ...

Quality Engineer

Greenville, MI · On-site

$60K - $70K/yr

Quality Engineer Position Summary We are seeking a Quality Engineer to support manufacturing operations by leading Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP ...

Quality Engineer

Saline, MI · On-site

$64K - $83K/yr

Emerald Technologies is seeking a Quality Engineer who is analytical, solutions‑driven, and ... Competitive medical, dental, and vision benefits 

Showing results 41-60

Quality Engineer Medical Device information

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

A Quality Engineer in the medical device industry is responsible for ensuring that medical devices meet all regulatory standards and quality requirements. They develop and implement quality assurance processes, perform risk assessments, and conduct inspections and audits to make sure products are safe and effective. Quality Engineers also collaborate with design, manufacturing, and regulatory teams to resolve quality issues and improve product reliability. Their work is crucial for maintaining compliance with standards such as ISO 13485 and FDA regulations.

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

To thrive as a Quality Engineer in the medical device industry, you need a strong background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and engineering principles, often supported by a relevant engineering degree. Familiarity with quality management systems (QMS), risk analysis tools (like FMEA), and certifications such as CQE (Certified Quality Engineer) are typically required. Attention to detail, problem-solving, and effective communication are critical soft skills for collaborating with cross-functional teams and ensuring product safety. These skills and qualifications are vital to maintain regulatory compliance, uphold product quality, and protect patient safety in a highly regulated environment.

How does a quality engineer in the medical device industry typically collaborate with cross-functional teams to ensure product compliance?

Quality Engineers in the medical device sector work closely with cross-functional teams such as design, manufacturing, regulatory affairs, and supply chain. They participate in design reviews, risk assessments, and process validations to ensure that products meet both internal quality standards and external regulatory requirements (such as FDA or ISO 13485). Regular collaboration involves reviewing documentation, addressing non-conformances, and implementing corrective actions. This teamwork is critical to proactively identify potential issues and maintain continuous product quality throughout the development and production lifecycle.

What is the difference between Quality Engineer Medical Device vs Quality Assurance Specialist Medical Device?

AspectQuality Engineer Medical DeviceQuality Assurance Specialist Medical Device
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, Six Sigma, ASQ certifications
Work EnvironmentDesign, development, manufacturing, and process improvementAuditing, compliance, documentation, and process verification
Employer & Industry UsageMedical device manufacturers, R&D labsMedical device companies, regulatory agencies, consulting firms

While both roles focus on quality in the medical device industry, a Quality Engineer Medical Device primarily works on product design, process development, and continuous improvement. In contrast, a Quality Assurance Specialist Medical Device emphasizes compliance, auditing, and ensuring adherence to regulatory standards. Both roles are essential for maintaining product safety and quality, but they differ in scope and daily responsibilities.

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 Quality Engineer Medical Device jobs in Michigan?

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

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

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

Infographic showing various Quality Engineer Medical Device 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.

$17.25 - $21.25/hr

Full-time

Re-posted 18 days ago


Job description

Job title : Medical Assembler
Client : Medical Device Manufacturing Company
Duration : 6 Months
Location : Grand Rapids, MI 49504
Shift : 3rd Shift (10:30 PM - 6:30 AM)
Description:
  • Assemble medical device components.
  • Build electronic and mechanical assemblies.
  • Follow diagrams and work instructions.
  • Use hand and power tools.
  • Perform quality inspections.
  • Conduct continuity checks.
  • Rework and test prototype assemblies.
  • Operate production equipment.
  • Report equipment issues.
  • Support packaging and production activities.
  • Assist with shipping, receiving, and inventory as needed.
  • Record production data accurately.

Required Qualifications:
  • Strong attention to detail.
  • Quality-focused mindset.
  • Ability to read and follow instructions.
  • Basic hand tool skills.
  • Ability to perform repetitive assembly work.
  • Good communication skills.
  • Comfortable working in a manufacturing environment.
  • No prior experience required.

Preferred Qualifications:
  • Manufacturing or assembly experience.
  • Experience with electronic or mechanical assemblies.
  • Familiarity with production equipment.
  • Basic knowledge of quality inspection processes.
  • Experience in a medical device or regulated manufacturing environment.

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