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Medical Device Designer Jobs in Michigan (NOW HIRING)

WilsonCTS

Staff Supplier Quality Engineer

Kalamazoo, MI · On-site

$60 - $65/hr

Ensure supplier quality activities align with applicable medical device, regulatory, and quality ... designs and supplier strategies. * Support quality improvement projects focused on supplier ...

SG2 Recruiting

Ada Embedded Engineer

Grand Rapids, MI

$126K - $166K/yr

Designing, developing, integrating, and maintaining software solutions using the Ada programming ... Experience supporting aerospace, defense, automotive, medical device, public safety, or other ...

Stryker

Product Safety Engineer

Portage, MI · On-site

$69K - $110K/yr

This role offers an opportunity to build expertise in product safety during medical device ... Ability to interpret, analyze, and test electrical designs * Proficiency with design and concept ...

SG2 Recruiting

Ada Embedded Engineer

Grand Rapids, MI · On-site

$126K - $166K/yr

Designing, developing, integrating, and maintaining software solutions using the Ada programming ... Experience supporting aerospace, defense, automotive, medical device, public safety, or other ...

Stryker

Product Safety Engineer

Grand Rapids, MI · On-site

$69K - $110K/yr

This role offers an opportunity to build expertise in product safety during medical device ... Ability to interpret, analyze, and test electrical designs * Proficiency with design and concept ...

Stryker

Senior Staff Electrical Engineer, R&D

Portage, MI · On-site

$102K - $171K/yr

... product designs. * Translate user, clinical, and business needs into system requirements ... Serve as a subject matter expert on medical device regulations, industry standards, design controls ...

Stryker

Senior Staff Electrical Engineer, R&D

Portage, MI · Hybrid

$102K - $171K/yr

... product designs. * Translate user, clinical, and business needs into system requirements ... Serve as a subject matter expert on medical device regulations, industry standards, design controls ...

Stryker

Senior Mechanical Engineer, R&D

Portage, MI · On-site

$77K - $129K/yr

... detailed mechanical designs. * Create prototypes and conduct testing to evaluate product ... Experience working in the medical device industry or another regulated industry. * Knowledge of ...

Stryker

Senior Mechanical Engineer, R&D

Portage, MI · On-site

$77K - $129K/yr

... detailed mechanical designs. * Create prototypes and conduct testing to evaluate product ... Experience working in the medical device industry or another regulated industry. * Knowledge of ...

Stryker

Staff Mechanical Engineer, R&D

Portage, MI · Hybrid

$89K - $148K/yr

Experience designing mechanical or electro-mechanical assemblies. * Proficiencyin engineering ... Previous experience in medical device or regulated industry. USN : $89,300 - $148,800 USD Annual ...

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Showing results 41-60

All JobsMedical Device Designer JobsMedical Device Designer Jobs in Michigan

Medical Device Designer information

See Michigan salary details

$65.8K

$111.8K

$163.9K

How much do medical device designer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for medical device designer in Michigan is $111,788.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,900.00 and $125,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical device designer?

To thrive as a Medical Device Designer, you need a strong background in biomedical engineering, product design, and knowledge of regulatory standards, typically supported by a relevant engineering degree. Proficiency with CAD software, rapid prototyping tools, and familiarity with FDA or ISO regulatory systems is essential. Creativity, problem-solving, collaboration, and attention to detail are vital soft skills for innovating and ensuring safety in device development. These skills and qualities are crucial for creating effective, compliant, and user-friendly medical devices that improve patient outcomes and meet industry standards.

What does a medical device designer do?

A Medical Device Designer is responsible for creating and developing medical devices and equipment used in healthcare settings. They combine knowledge of engineering, biology, and design principles to ensure products are safe, effective, and user-friendly. Their role involves working closely with healthcare professionals, conducting research, prototyping, and adhering to regulatory standards throughout the design and development process. Medical Device Designers help bring innovative medical solutions to market that improve patient care and outcomes.

What are some common challenges faced by medical device designers when balancing innovation with regulatory compliance?

Medical device designers often face the challenge of creating innovative, user-friendly products while ensuring strict adherence to regulatory standards such as FDA or ISO requirements. Balancing creativity with compliance can be demanding, as any design change may necessitate additional documentation, testing, and validation. Designers must closely collaborate with regulatory specialists, engineers, and clinicians to ensure their solutions are both safe and effective. Staying up-to-date with changing regulations and incorporating feedback from multidisciplinary teams are key aspects of overcoming these challenges.
What are popular job titles related to Medical Device Designer jobs in Michigan? For Medical Device Designer jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Medical Device Designer jobs in Michigan look for? The top searched job categories for Medical Device Designer jobs in Michigan are:
Medical Device Designer jobs near you
Infographic showing various Medical Device Designer job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $111,788 per year, or $53.7 per hour.

Staff Supplier Quality Engineer

WilsonCTS

Kalamazoo, MI • On-site

$60 - $65/hr

Contractor

Posted 17 days ago

Job description

Job Title: Staff Engineer, Supplier Quality Engineering
Employment Type: 18-month contract
Work Location: Kalamazoo, Michigan
Work Arrangement: Onsite, with travel required
Hours: 40 hours per week
Pay Rate: $60.00-$65.00 per hour

Position Summary

We are seeking an experienced Staff Supplier Quality Engineer to support supplier quality engineering activities within a highly regulated environment.

The Staff Supplier Quality Engineer will serve as a key liaison between suppliers and internal teams to drive supplier quality performance, continuous improvement, and quality system effectiveness. This role will support supplier quality issues, supplier audits, supplier performance evaluations, quality improvement projects, and supplier quality system assessments.

The successful candidate will work closely with internal stakeholders, strategic sourcing, auditing, supplier development teams, and external suppliers to ensure supplier processes, quality systems, and performance meet quality and regulatory requirements.

Key Responsibilities
Supplier Quality and Performance Management
  • Serve as a liaison between suppliers and internal teams to support supplier quality performance and continuous improvement.
  • Support supplier quality issues by providing technical guidance, problem-solving support, and quality engineering expertise.
  • Assess and critique supplier processes, control documentation, and quality management systems.
  • Drive improvements within supplier quality management systems and supplier processes.
  • Support tracking, reporting, and analysis of supplier performance KPIs and quality metrics.
  • Articulate supplier performance results, trends, risks, and improvement opportunities to appropriate levels of management.
  • Maintain and track completion of supplier action plans and corrective actions.

Supplier Audits and Quality System Support
  • Support supplier audits and quality system assessments.
  • Participate in audits required by the organization, including supplier audits that may require travel.
  • Provide support during third-party audits related to supplier quality engineering deliverables.
  • Evaluate supplier compliance with applicable quality standards, regulatory requirements, and internal expectations.
  • Collaborate with auditing and supplier development groups to understand supplier capabilities and competencies.
  • Ensure supplier quality activities align with applicable medical device, regulatory, and quality system requirements.

Continuous Improvement and Problem Solving
  • Propose and develop effective supplier quality improvement plans.
  • Work with suppliers to implement corrective and preventive actions and drive sustainable improvements.
  • Provide problem-solving expertise at company sites and supplier locations as needed.
  • Identify and execute cost-reduction opportunities with suppliers.
  • Transfer lessons learned from the supply base to internal teams for inclusion in future product designs and supplier strategies.
  • Support quality improvement projects focused on supplier performance, process capability, and risk reduction.
Cross-Functional Collaboration
  • Partner with strategic sourcing, supplier development, auditing, engineering, quality, operations, and regulatory teams.
  • Act as a single point of contact for strategic business partners and participate in supplier reviews as needed.
  • Communicate effectively with suppliers and internal stakeholders at various levels of the organization.
  • Represent the organization professionally during supplier visits, audits, and quality discussions.
  • Support collaborative team-based work initially, with increasing autonomy once fully trained and aligned on key KPIs.
Technical Leadership and Process Ownership
  • Serve as a subject matter expert for assigned commodities or supplier quality areas.
  • Share supplier quality expertise across the global organization.
  • Serve as a process owner and support standardization of supplier quality-related processes.
  • Train, mentor, and assist in the development of less experienced engineers.
  • Work with a tenured team of supplier quality engineers and assigned mentors.
  • Perform additional supplier quality engineering duties as assigned.
Required Qualifications
  • Bachelor's degree in Science, Engineering, or a related discipline preferred, or equivalent years of relevant experience.
  • Minimum of 4 years of experience in quality, manufacturing, supplier quality, or a highly regulated environment.
  • 3-5 years of experience in a regulated industry required, with preference for medical device, pharmaceutical, or automotive environments.
  • 3-5 years of supplier-facing experience.
  • Lead Quality Auditor qualification required, such as ISO 13485, 21 CFR Part 820, or a comparable standard/regulation.
  • Strong written and verbal communication skills.
  • Strong interpersonal, negotiation, and stakeholder management skills.
  • Ability to represent the organization professionally during supplier visits and audits.
  • Ability to travel for supplier audits, mostly short trips across the Midwest, sometimes with limited notice.
  • Ability to work 40 hours per week.
Preferred Qualifications
  • Active Lead Quality Auditor qualification strongly preferred; expired qualification may be considered with relevant recent audit experience.
  • ASQ certification such as CQE, CMQ/OE, or PE.
  • Lean Six Sigma Green Belt or Black Belt certification.
  • Quality engineering experience.
  • Experience using TrackWise.
  • Working knowledge of FMEA, validation programs, and statistical process control.
  • Knowledge of manufacturing processes, prints, tolerancing, statistics, and project management.
  • Understanding of U.S. and international medical device regulations.
  • Experience influencing supplier quality performance and driving supplier corrective actions.
  • Experience supporting third-party audits or regulatory inspections.
Additional Details
  • Travel is required for supplier audits, primarily across the Midwest.
  • Candidates should be flexible for short trips and occasional limited-notice travel.
  • Preferred candidate locations include Michigan, Indiana, Ohio, and Illinois.
  • The role will begin with collaborative team-based work and training.
  • Once trained, the contractor will have more autonomy while still being supported by the manager to ensure key KPIs are met.
  • The selected candidate will work with a tenured team of approximately 10 engineers and will be set up with mentors.

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