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Medical Device Product Development Jobs in Michigan

Three Point Solutions

Medical Assembler

Grand Rapids, MI · On-site

$18 - $20/hr

Production Documentation * Teamwork Preferred Skills: * Manufacturing Experience * Medical Device Assembly * Mechanical/Electronic Components * Production Processes * Semi-Automated Equipment ...

Three Point Solutions

Medical Assembler

Dexter, MI · On-site

$18 - $22/hr

Medical device assembly experience. Work Environment: * Manufacturing production environment. * Supports assembly, processing, packaging, and distribution operations. * May operate semi-automatic ...

Three Point Solutions, Inc.

Medical Assembler

Dexter, MI · On-site

$17.25 - $21/hr

... medical device components in a manufacturing environment. • Perform production, inspection, testing, and rework activities following standard operating procedures. • Support manufacturing ...

Three Point Solutions

Medical Assembler

Grand Rapids, MI

$17.25 - $21.25/hr

Report equipment issues or production abnormalities to supervisors. * Work overtime, including occasional Saturdays, as required. Required Skills: * Medical device assembly or manufacturing ...

Three Point Solutions, Inc.

Medical Assembler

Dexter, MI · On-site

$17.25 - $21/hr

Medical device assembly experience. Work Environment: * Manufacturing production environment. * Supports assembly, processing, packaging, and distribution operations. * May operate semi-automatic ...

Three Point Solutions

Medical Assembler

Grand Rapids, MI

$17.25 - $21.25/hr

Report equipment issues or production abnormalities to supervisors. * Work overtime, including occasional Saturdays, as required. Required Skills: * Medical device assembly or manufacturing ...

Benteler

Product Development Engineer

Grand Rapids, MI · On-site

Medical || United States : Training || United States : Vacation || United States : Vision || United ... As a Product Development Engineer, you will play a crucial role in the design, development, and ...

Three Point Solutions

Medical Assembler

Grand Rapids, MI

$17.25 - $21.25/hr

Medical Device Assembly * Mechanical/Electronic Components * Production Processes * Semi-Automated Equipment Education: * High School Diploma or equivalent preferred. Experience: * No prior ...

Three Point Solutions

Medical Assembler

Grand Rapids, MI

$17.25 - $21.25/hr

Medical Device Assembly * Mechanical/Electronic Components * Production Processes * Semi-Automated Equipment Education: * High School Diploma or equivalent preferred. Experience: * No prior ...

Able Medical Devices

CNC Programmer (Milling)

Gwinn, MI · On-site

$25.75 - $35.25/hr

... Medical Device Implants and Instruments (or equivalent); thorough understanding of production and product development regulations and Quality Control processes, including gaging and OGP operation ...

Three Point Solutions

Medical Assembler

Dexter, MI

$17.25 - $21/hr

Medical device assembly experience. Work Environment: * Manufacturing production environment. * Supports assembly, processing, packaging, and distribution operations. * May operate semi-automatic ...

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All JobsMedical Device Product Development JobsMedical Device Product Development Jobs in Michigan

Medical Device Product Development information

What is a medical device product development?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in medical device product development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in medical device product development?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

What are the most commonly searched types of Medical Device Product Development jobs in Michigan? The most popular types of Medical Device Product Development jobs in Michigan are:
What are popular job titles related to Medical Device Product Development jobs in Michigan? For Medical Device Product Development jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Medical Device Product Development jobs in Michigan look for? The top searched job categories for Medical Device Product Development jobs in Michigan are:
What cities in Michigan are hiring for Medical Device Product Development jobs? Cities in Michigan with the most Medical Device Product Development job openings:
Medical Device Product Development jobs near you
Infographic showing various Medical Device Product Development job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 1% Temporary, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Senior Electrical Engineer- EMC/Compliance

Stryker

Ann Arbor, MI • On-site

$77K - $129K/yr

Full-time

Re-posted 14 days ago

Job description

Work Flexibility: Onsite

Stryker is seeking a Senior Compliance Engineer, EMC to support electromagnetic compatibility testing and compliance activities for new product development and/or sustaining engineering, contributing to successful global product launches and ongoing regulatory compliance for Stryker Medical. Develop and execute EMC test plans and support design reviews. Apply EMC standards and test methods for medical devices, building proficiency in IEC 6060112 and related global requirements. Collaborate with design, quality, and regulatory teams to identify and resolve EMC compliance needs throughout the product lifecycle.

This role is an individual contributor position focused on developing technical depth in EMC testing, standards application, and compliance processes. The EMC Engineer builds hands-on expertise through testing, analysis, and cross-functional collaboration while growing toward increased technical knowledge and responsibility.

What You Will Do

  • Lead EMC compliance strategy for new product development and sustainment programs, translating global standards into clear requirements and ensuring successful global market access.

  • Partner with design and subject matter experts throughout the product lifecycle to develop compliance plans, embed EMC best practices, and evaluate designs for EMC performance and risk.

  • Develop and execute efficient EMC assessment strategies using design reviews, risk-based evaluations, and data-driven approaches to support product compliance.

  • Investigate EMC compliance issues, perform root cause analysis, and drive effective mitigation strategies to resolve technical challenges.

  • Serve as the EMC compliance lead for cross-functional programs, exercising independent judgment, influencing technical direction, and driving EMI/EMC processes and best practices across engineering disciplines while managing external certification laboratories and NRTL partners.

  • Up to 20%, as required to support projects, partners, and industry engagement.

What You Need (Required Qualifications)

  • Bachelor's degree in electrical engineering or related discipline.

  • 2+ years of experience required.

Preferred Qualifications

  • Experience with product safety regulatory certification for major standards bodies and frameworks (e.g., IEC, AAMI, and related schemes).

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

  • Experience working with and managingthird-partycertification laboratories (e.g., UL, TUV, CSA, Intertek).

  • Experience withdevice regulatorycertification involving safety, EMC, and/or wireless standards.

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

  • 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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