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Research And Development Engineer Medical Device Jobs in Michigan

Atego

Software Engineer

Zeeland, MI · On-site

This position will interface with Project Engineering, Hardware Engineering, Software Test, Program Management, and Research & Development. The following qualifications are required The following ...

pregis

Product Development Engineer

Grand Rapids, MI · On-site

Product Development Engineer Anderson, SC Position Description Reporting to the VP of Technology ... Support product development team in completion of customer trial orders * Assist R&D in completion ...

Biovire

Manager, Process Development

Brighton, MI · On-site

$100K - $120K/yr

Manager, Process Development Engineering Organization Brighton, Michigan Biovire is advancing ... medical device manufacturing. This role leads a team of Process Engineers and ensures that ...

Biovire

Manager, Process Development

Brighton, MI

Manager, Process Development Engineering Organization Brighton, Michigan Biovire is advancing ... medical device manufacturing. This role leads a team of Process Engineers and ensures that ...

Pregis

Product Development Engineer

Grand Rapids, MI · On-site

Product Development Engineer Anderson, SC Position Description Reporting to the VP of Technology ... Support product development team in completion of customer trial orders * Assist R&D in completion ...

Stryker

Associate Manager, R&D Engineering

Portage, MI · On-site

$102K - $171K/yr

As an Associate Manager, R&D Engineering you'll support the Product Engineering team by leading a ... Familiarity with the healthcare or medical device industry. * Proven ability to deliver programs on ...

Weiss-Aug MedPharma

Weiss-Aug, is a leading provider of advanced manufacturing and engineering solutions with advanced ... We're currently seeking a passionate and skilled Quality Systems Manager - Medical Device ...

New

Valeo

Software Engineer

Troy, MI · On-site

Job: R&D Engineer Organization: Schedule: Full time Employee Status: Regular Job Type: Job Posting Date: 2026-08-19 Join Us ! Being part of our team, you will join: - one of the largest global ...

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Research And Development Engineer Medical Device information

What does a research and development engineer do in the medical device industry?

A Research and Development (R&D) Engineer in the medical device industry is responsible for designing, developing, and testing new medical devices and technologies. They work closely with cross-functional teams to ensure products meet regulatory standards, are safe for patient use, and address clinical needs. Their tasks may include prototyping, conducting experiments, analyzing data, and collaborating with manufacturing teams to bring products from concept to market. R&D Engineers also stay updated on technological advancements and regulatory changes to ensure innovation and compliance.

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

To excel as a Research and Development Engineer in Medical Devices, you need a solid background in biomedical engineering or a related field, strong problem-solving skills, and experience with product development cycles. Familiarity with CAD software, prototyping tools, regulatory standards like ISO 13485, and relevant certifications (such as Six Sigma) is highly valued. Excellent teamwork, creativity, and effective communication are crucial soft skills for collaborating across multidisciplinary teams and driving innovation. These competencies ensure the design and launch of safe, effective, and compliant medical devices that improve patient outcomes.

What are some common challenges faced by research and development engineers in the medical device industry?

Research and Development Engineers in the medical device industry often face challenges such as navigating complex regulatory requirements, managing tight project timelines while ensuring product safety and efficacy, and collaborating with cross-functional teams like quality assurance and clinical affairs. Additionally, adapting to rapid technological advancements and integrating feedback from clinicians and end-users into the design process can be demanding. These challenges require strong problem-solving skills, adaptability, and effective communication to deliver innovative and compliant medical devices.

What is the difference between Research And Development Engineer Medical Device vs Quality Assurance Engineer Medical Device?

AspectResearch And Development Engineer Medical DeviceQuality Assurance Engineer Medical Device
Primary FocusDesigning, developing, and testing new medical device productsEnsuring products meet quality standards and regulatory requirements
Required CredentialsEngineering degree, knowledge of product developmentEngineering or science degree, knowledge of quality systems
Work EnvironmentResearch labs, product development teamsManufacturing facilities, quality control departments
Industry UsageInvolved in innovation and product creationInvolved in compliance, validation, and process improvement

While both roles require engineering knowledge and are integral to the medical device industry, Research And Development Engineers focus on creating and testing new products, whereas Quality Assurance Engineers ensure these products meet safety and quality standards throughout production.

What are popular job titles related to Research And Development Engineer Medical Device jobs in Michigan?

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

What job categories do people searching Research And Development Engineer Medical Device jobs in Michigan look for?

The top searched job categories for Research And Development Engineer Medical Device jobs in Michigan are:

What cities in Michigan are hiring for Research And Development Engineer Medical Device jobs?

Cities in Michigan with the most Research And Development Engineer Medical Device job openings:

Research And Development Engineer Medical Device jobs near you
Infographic showing various Research And Development Engineer Medical Device job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Senior Compliance Engineer - Digital Health

Stryker

Grand Rapids, MI • Hybrid

$77K - $129K/yr

Full-time

Posted 11 days ago

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

131st of 494 rated machine equipment manufacturers

Job description

Work Flexibility: Hybrid

The Senior Compliance Engineer will provide dedicated compliance engineering support for Stryker Medical's growing Smart Care portfolio. Software as/in a Medical Device (SaMD + SiMD) will comprise the portfolio core along with supporting hardware, sensors, and customer applications. Partner with diverse teams to drive best in market digital health solutions supporting the caregiver, patient and families. Grow and adapt the technology & test roadmap to align with business ambition and future technology integration. Support digital and connected ecosystems through standards interpretation and test method mastery. Ensure state of the art interpretation of global compliance standards for medical and non-medical markets to enable globalization portfolio growth.

This is a highly specialized individual contributor role that requires deep technical expertise and professional judgment. The Staff Compliance Engineer - Digital serves as a technical thought leader, providing guidance, influence, and direction across product development, certification strategy, and organizational best practices.

Check out the products you'll support here: Smart Care | Stryker

This role is hybrid expecting a minimum of 3 days a week in the Portage, MI office, typically Monday through Wednesday.

What You Will Do

  • Lead product compliance strategy for new product development and sustaining engineering activities across the Smart Care portfolio.

  • Translate global regulatory and compliance requirements into design inputs, verification plans, and market access strategies.

  • Drive compliance activities throughout the product lifecycle, from concept development through verification, validation, and commercialization.

  • Assess compliance risks, predicate product considerations, and emerging requirements to support informed design and business decisions.

  • Partner with cross-functional teams to integrate compliance requirements into system architecture, product design, and technology roadmaps.

  • Define compliance test strategies, methods, operating environments, and worst-case conditions to ensure robust product evaluations.

  • Manage external testing laboratories, certification bodies, and third-party partners to support global certifications and regulatory submissions.

  • Serve as a technical compliance subject matter expert, providing guidance during design reviews, risk assessments, and development activities.

  • Influence organizational compliance practices by supporting procedure development, technical reviews, innovation opportunities, and cross-business initiatives.

  • Collaborate with stakeholders, and business units to ensure compliance strategies align with user needs, product classifications, and market requirements.

What You Need (Required Qualifications)

  • Bachelor's degree in Computer Science, Software/Electrical Engineering or related discipline.

  • 4+ years of compliance engineering experience required.

Preferred Qualifications

  • Master's degree in Computer Science, Software/Electrical Engineering or related discipline.

  • Experience with product safety regulatory certification for major standards bodies and frameworks (IEC 60601-1, IEC 60601-1-8, FCC Requirements, IEC 62368-1 and others)

  • Experience with medical device product development lifecycle, including design controls and risk management.

  • Experience working with and managing third-party certification laboratories (e.g., UL, TUV, CSA, Intertek).

  • Experience with device regulatory certification involving safety, EMC, and/or wireless standards.

  • Able to balance business and technical challenges to achieve financial outcomes.

  • Knowledge of telecom/non-medical device standards.

  • Familiarity with different software development life cycles.

  • Basic knowledge of regulatory certification and device submission processes.

  • Demonstrated ability to work independently and effectively in a matrixed organization.

  • Demonstrated ability to effectively work cross-functionally with other departments, including Research & Development, Regulatory Affairs, and Marketing.

  • Strong written, verbal, and interpersonal communication skills with the ability to influence without authority.

$77,700 - $129,500 USD Annual

Travel Percentage: 20%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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