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Medical Device Product Development Jobs in Michigan

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 ...

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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, 76% Full Time, 16% Part Time, 6% Contract, and 1% Nights. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution.

Staff Electrical Engineer - PCB Layout & Component Library Support

Stryker

Portage, MI • On-site

$89K - $148K/yr

Full-time

Re-posted 6 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 495 rated machine equipment manufacturers

Job description

Work Flexibility: Hybrid
Stryker is seeking a Staff Electrical Engineer who can deliver high-quality PCB layout, ECAD component library support, and component engineering for medical device product development. This role converts schematics and design inputs into manufacturable PCB/PCBA outputs, maintains controlled ECAD library data, supports component lifecycle and BOM reviews, and partners with engineering, manufacturing, supply chain, and external PCBA suppliers to resolve design and production issues. The ideal candidate has strong Altium and OrCAD/Allegro capability, practical PCB/PCBA manufacturing knowledge, and experience with DFM/DFT, Valor, and Silicon Expert or equivalent tools.
What You Will Do
  • Independently design and develop PCB layouts and related ECAD outputs for medical device components, sub-systems, prototypes and production releases.
  • Translate schematics, design inputs and system constraints into manufacturable PCB/PCBA designs using Altium Designer, OrCAD/Allegro and applicable legacy ECAD platforms.
  • Optimise PCB designs for manufacturability, assembly, testability, signal and power integrity, EMI/EMC, thermal performance, mechanical fit and supplier capability.
  • Create, review and maintain controlled ECAD library content, including schematic symbols, footprints, component models and associated documentation.
  • Generate and review PCB fabrication and assembly packages, including Gerber and ODB++ files, drawings, BOM outputs, release packages and engineering change documentation.
  • Lead advanced problem solving and root cause analysis related to PCB design, manufacturing, yield, quality, reliability and component issues.
  • Perform component engineering activities, including component selection, BOM reviews, lifecycle and obsolescence assessments, alternate sourcing and supply-chain support.
  • Develop and improve ECAD design guidelines, library governance, review processes, databases and tools, including DFM/DFT, manufacturing-readiness, automation and emerging AI-assisted workflows.
  • Collaborate across Electrical Engineering, R&D, Quality, Manufacturing, Supply Chain, Advanced Operations and external manufacturing partners, providing technical leadership and mentoring others in ECAD and PCB design best practices.

What You Need (Required Qualifications)
  • Bachelor's degree in EE or related discipline & 4+ years of work experience.
  • Demonstrated experience in PCB layout design, ECAD component library development, PCB/PCBA documentation, component engineering, or related electrical CAD work.

Preferred Qualifications
  • Understanding of ECAD PCB layout, component libraries, PCB/PCBA manufacturing methods, and common failure modes.
  • Ability to translate schematics, design inputs, and system constraints into manufacturable PCB/PCBA layout outputs.
  • Proficiency with Altium Designer and OrCAD/Allegro; familiarity with legacy ECAD platforms preferred.
  • Working knowledge of controlled ECAD documentation, library governance, and engineering change/release processes.
  • Practical understanding of DFM/DFT, PCB manufacturing-readiness, component lifecycle, BOM review, and obsolescence risk.
  • Ability to review PCB/PCBA designs for manufacturability, testability, EMI/EMC, thermal performance, mechanical fit, and system-level interactions.
  • Experience with Valor, Silicon Expert, or equivalent PCB analysis and component lifecycle tools preferred.

$89,300 - $148,800 USD Annual
Travel Percentage: 10%
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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