ZipRecruiter

Log In

1

Medical Device Research And Development Jobs in Michigan

Stryker

Staff Mechanical Engineer, R&D

Portage, MI · On-site

$89K - $148K/yr

Hybrid Staff Mechanical Engineer, R&D Portage, MI Join a team developing innovative medical device technologies from concept through commercialization. This role provides the opportunity to ...

Stryker

Staff Mechanical Engineer, R&D

Portage, MI · On-site

$89K - $148K/yr

Hybrid Staff Mechanical Engineer, R&D Portage, MI Join a team developing innovative medical device technologies from concept through commercialization. This role provides the opportunity to ...

Mitovation

Be Seen First

Systems Engineer - Medical Device Company

Ann Arbor, MI · On-site

$110K - $140K/yr

The technology originated from mitochondrial biology research at Wayne State University and the ... New system design / development: * Translate clinical and user needs into system, subsystem, and ...

Stryker

Senior Staff Mechanical Engineer, R&D

Portage, MI · On-site

$102K - $171K/yr

The Senior Staff R&D Engineer Lead serves as a technical leader, guiding design decisions ... Experience supporting medical device development within a regulated environment. $102,600 - $171 ...

Stryker

Senior Staff Mechanical Engineer, R&D

Portage, MI · On-site

$102K - $171K/yr

The Senior Staff R&D Engineer Lead serves as a technical leader, guiding design decisions ... Experience supporting medical device development within a regulated environment. $102,600 - $171 ...

Aptar Group

Business Development Manager

Midland, MI · On-site +1

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

Aptar Group

Business Development Manager

Midland, MI · On-site

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

Stryker

Staff Mechanical Engineer, R&D

Portage, MI · 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 ...

Stryker

Staff Mechanical Engineer, R&D

Portage, MI · 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 ...

Stryker

Senior Manager, Engineering - R&D

Portage, MI · On-site

$135K - $225K/yr

Onsite Are you passionate about leading high-performing teams and delivering impactful innovation in the medical device industry? Join us as a Senior Manager, Engineering in R&D and help shape the ...

Stryker

Senior Manager, Engineering - R&D

Portage, MI · On-site

$135K - $225K/yr

Onsite Are you passionate about leading high-performing teams and delivering impactful innovation in the medical device industry? Join us as a Senior Manager, Engineering in R&D and help shape the ...

next page

Showing results 1-20

All JobsMedical Device Research And Development JobsMedical Device Research And Development Jobs in Michigan

Medical Device Research And Development information

What is medical device research and development?

Medical device research and development (R&D) is the process of designing, creating, testing, and improving medical devices used for diagnosing, treating, or preventing health conditions. This field combines engineering, biology, and medicine to develop innovative tools ranging from simple instruments to complex implantable devices. Professionals in this area work on everything from concept development and prototyping to clinical trials and regulatory approval. Their work ensures that medical devices are safe, effective, and meet strict regulatory standards before reaching patients.

What are some typical challenges faced by professionals in medical device research and development, and how can these be managed?

Professionals in Medical Device Research and Development often encounter challenges such as navigating complex regulatory requirements, balancing innovation with safety, and coordinating cross-functional teams. Managing these challenges involves staying current with FDA and international regulations, fostering open communication between engineering, clinical, and regulatory teams, and maintaining rigorous documentation throughout the development process. Strong project management skills and a collaborative mindset are key to overcoming these obstacles and ensuring successful product development.

What are the key skills and qualifications needed to thrive in medical device research and development, and why are they important?

To thrive in Medical Device Research and Development, you need a solid background in engineering or life sciences, along with experience in product design and knowledge of regulatory standards. Familiarity with CAD software, prototyping tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong problem-solving skills, creativity, and effective teamwork set standout professionals apart in this field. These skills and qualities are crucial to ensure innovative, safe, and compliant medical devices that meet both clinical needs and regulatory requirements.

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

AspectMedical Device Research And DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications in R&DQuality certifications, regulatory training
Work EnvironmentLabs, design teams, product developmentInspection facilities, compliance departments
Employer & Industry UsageManufacturers, biotech firms, innovation labsRegulatory agencies, manufacturing companies
Search & Comparison IntentInnovation, product development, prototypingCompliance, testing, product validation

Medical Device Research And Development focuses on designing and developing new medical devices, emphasizing innovation and prototyping. In contrast, Medical Device Quality Assurance ensures products meet safety and regulatory standards through testing and compliance. Both roles are essential in the medical device industry but serve different stages of the product lifecycle.

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

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

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

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

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

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

Medical Device Research And Development jobs near you
Infographic showing various Medical Device Research And Development 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.

Staff Mechanical Engineer, R&D

Stryker

Portage, MI • On-site

$89K - $148K/yr

Full-time

Re-posted 4 hours ago

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

130th of 495 rated machine equipment manufacturers

Job description

Work Flexibility: Hybrid
Staff Mechanical Engineer, R&D
Portage, MI
Join a team developing innovative medical device technologies from concept through commercialization. This role provides the opportunity to contribute across the product development lifecycle, applying engineering expertise to the design, development, testing, and verification of medical device components and systems. The position partners closely with cross-functional teams to support product quality, regulatory compliance, and successful project execution.
Work Flexibility:
Hybrid: candidates must reside within commuting distance of Portage, MI and be able to work onsite several days per week.
What You Will Do
  • Design, develop, modify, and verify medical device components, modules, and sub-systems in accordance with design requirements.
  • Translate user and clinical needs into design inputs, specifications, and system-level design solutions.
  • Plan, build, and evaluate prototypes and testing methods to verify product performance and design requirements.
  • Investigate product design issues, perform technical analyses, and implement design improvements.
  • Apply knowledge of customer needs, market insights, and clinical procedures to support product development activities.
  • Create, maintain, and refine engineering documentation, including design history records, specifications, drawings, and test protocols.
  • Ensure compliance with applicable medical device regulations, design controls, risk management requirements, and quality system procedures.
  • Collaborate with Quality, Manufacturing, Regulatory Affairs, Clinical, Marketing, and Project Management teams to advance projects through development and launch milestones.

What You Will Need
Required Qualifications
  • Bachelor of Science degree in Engineering, Mechanical Engineering, Biomedical Engineering, or a related engineering discipline.
  • Minimum 4 years of engineering experience in Research & Development (R&D)
  • Experience creating engineering drawings and technical documentation.
  • Experience supporting product verification and testing activities.

Preferred Qualifications
  • Experience developing mechanical or electro-mechanical assemblies using Design for Manufacturability principles.
  • Experience using computer-aided design tools and applying Geometric Dimensioning and Tolerancing (GD&T).
  • Experience applying material selection and manufacturing process knowledge to product design.
  • Experience working within a regulated industry environment, including design controls and risk management processes.

  • $89,300 - $148,800 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.

What Stryker employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply