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Research And Development Engineer Medical Device Jobs in Michigan

Medical Device Assembly

Wixom, MI ยท On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Medical Device Assembly

Wixom, MI ยท On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Medical Device Assembly

Wixom, MI ยท On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

The Specialist Research and Development (R&D) Engineer for Pumps and Seals is responsible for ... PhD Benefits Starting on Day 1: * Medical, Dental & Vision Insurance (including FSA and HSA options)

Senior Mechanical Engineer, R&D

Portage, MI ยท On-site

$77K - $129K/yr

Work Flexibility: Hybrid Senior Mechanical Engineer, R&D Portage, MI As a Senior Mechanical ... Experience working in the medical device industry or another regulated industry. * Knowledge of ...

Senior Mechanical Engineer, R&D

Portage, MI ยท On-site

$77K - $129K/yr

Work Flexibility: Hybrid Senior Mechanical Engineer, R&D Portage, MI As a Senior Mechanical ... Experience working in the medical device industry or another regulated industry. * Knowledge of ...

Staff Mechanical Engineer, R&D

Portage, MI ยท Hybrid

$89K - $148K/yr

As a Staff Mechanical Engineer in our Research & Development team, you willsupport multiple ... Previous experience in medical device or regulated industry. USN : $89,300 - $148,800 USD Annual ...

Staff Mechanical Engineer, R&D

Portage, MI ยท On-site

$89K - $148K/yr

As a Staff Mechanical Engineer in our Research & Development team, you will support multiple ... Previous experience in medical device or regulated industry. USN : $89,300 - $148,800 USD Annual ...

... Medical Device applications (e.g., enteral feeding bags, trocars, lab diagnostic testing, endoscopic devices). * Develop strong relationships within key accounts across functions (R&D/engineering ...

... Medical Device applications (e.g., enteral feeding bags, trocars, lab diagnostic testing, endoscopic devices). * Develop strong relationships within key accounts across functions (R&D/engineering ...

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

Be Seen First

Experience supporting medical device development in a regulated environment. * Experience developing product safety documentation, compliance strategies, and engineering test plans. * Working ...

New

Be Seen First

Experience supporting medical device development in a regulated environment. * Experience developing product safety documentation, compliance strategies, and engineering test plans. * Working ...

New

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

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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 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 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 are the key skills and qualifications needed to thrive as a Research and Development Engineer in Medical Devices, and why are they important?

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 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:
Infographic showing various Research And Development Engineer Medical Device job openings in Michigan as of July 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, 5% Contract, and 1% Nights. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution.

Staff Software Systems Engineer- Medical Device

Stryker

Portage, MI โ€ข On-site

$102K - $171K/yr

Full-time

Re-posted 8 days ago


Job description

Work Flexibility: Hybrid
Stryker is seeking a technical leader responsible for guiding the development of complex, software-driven medical device systems. This position supports our Neurosurgical group and operates at the intersection of systems engineering and software development, ensuring alignment among stakeholder needs, system architecture, regulatory requirements, and product implementation. The role also ensures end-to-end traceability from stakeholder needs through software requirements and verification, in full compliance with design controls and the software development lifecycle.
What You Will Do
  • Translate user, clinical, and system-level needs into clear, traceable high level software requirements.
  • Contribute to early concept development and system architecture decisions, driving resolution of complex design challenges.
  • Drive software system integration, verification, and validation activities to ensure performance, quality, and safety objectives are met.
  • Establish and maintain end-to-end traceability across requirements, architecture, implementation, testing, and defect management.
  • Coach and guide teams in developing high-quality, testable, and compliant requirements.
  • Partner with Agile software development teams to prioritize features and enable efficient, predictable delivery.
  • Collaborate cross-functionally with Quality, Regulatory, Project Management, and multi-disciplinary R&D teams to ensure alignment and execution.
  • Support Voice of Customer (VOC) activities and incorporate clinical and customer insights into system design and development.
  • Contribute to Design History File (DHF) documentation and ensure adherence to medical device regulations, design controls, and quality system requirements.

What You Need (Required Qualifications)
  • Bachelor's degree in Software Engineering/ Computer Science or related discipline & 4+ years of work experience

Preferred Qualifications (Strongly Desired)
  • Experience developing and optimizing complex software systems.
  • Advanced knowledge of Requirements Management and System Modeling Tools.
  • Ability to communicate complex technical concepts and plans clearly.
  • Experience influencing SDLC and ALM/traceability processes and best practices.
  • Ability to estimate effort, timelines, and resources for software implementation.
  • Understanding of regulatory and compliance requirements within the SDLC.
  • Knowledge of software analysis techniques, including static/dynamic analysis and code coverage.

$102,600 - $171,000 USD Annual
Travel Percentage: 30%
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.