1

Medical Device Systems Engineer Jobs (NOW HIRING)

Systems Verification & Validation Engineer, R&D (Medical Devices) This role focuses on leading ... Ensure compliance with relevant medical device industry regulations and standards, including FDA ...

New

Systems Verification & Validation Engineer, R&D (Medical Devices) This role focuses on leading ... Ensure compliance with relevant medical device industry regulations and standards, including FDA ...

New

Sr. Systems Engineer

Boston, MA ยท Hybrid

$113K - $155K/yr

Gardner Resources Consulting, LLC is seeking a Sr. Systems Engineer to support CVS Health's regulated medical device and clinical technology initiatives. The ideal candidate will have strong ...

Sr. Systems Engineer

Boston, MA ยท Hybrid

$113K - $155K/yr

Gardner Resources Consulting, LLC is seeking a Sr. Systems Engineer to support CVS Health's regulated medical device and clinical technology initiatives. The ideal candidate will have strong ...

Systems Engineer MedTech / Medical Devices / SF Bay Representing a pioneering medical device company that specializes in the development of unique life-saving Medical Technologies. They are currently ...

Medical Device Assembler

Madison, WI ยท On-site

$23 - $24/hr

Ensure work is completed in compliance with company quality system and medical device regulations ... Engineering group as required. Working Conditions: Clean, temperature controlled environment.

Medical Device Assembly

Wixom, MI ยท On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Familiarity with GMP, ISO 13485, or FDA quality system regulations is a plus * Ability to stand ...

Showing results 41-60

Medical Device Systems Engineer information

See salary details

$53.5K

$127.2K

$167K

How much do medical device systems engineer jobs pay per year?

As of Sep 6, 2026, the average yearly pay for medical device systems engineer in the United States is $127,215.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What does a medical device systems engineer do?

A Medical Device Systems Engineer is responsible for designing, developing, and integrating complex medical devices and systems. They work closely with multidisciplinary teams to ensure that devices meet regulatory standards, are safe for patients, and function as intended. Their role often includes system architecture, requirements analysis, risk management, and verification and validation testing. They also collaborate with clinicians and regulatory bodies to ensure compliance with healthcare standards. Overall, their work is crucial in bringing innovative medical technologies from concept to market.

How does a medical device systems engineer typically collaborate with cross-functional teams during product development?

Medical Device Systems Engineers play a central role in coordinating with interdisciplinary teams such as mechanical, electrical, software, and quality assurance engineers, as well as regulatory and clinical experts. They are responsible for integrating various subsystems, ensuring the final device meets both technical and regulatory requirements. This often involves leading design reviews, facilitating communication between specialties, and translating user needs into system specifications. Collaboration is key, as engineers must address feedback from multiple stakeholders and ensure seamless system integration throughout the product development lifecycle.

What are the key skills and qualifications needed to thrive as a medical device systems engineer, and why are they important?

To thrive as a Medical Device Systems Engineer, you need a strong background in biomedical engineering, systems engineering principles, and regulatory knowledge, often supported by a relevant engineering degree. Familiarity with CAD software, embedded systems, FDA/ISO standards, and risk management tools is typically required. Exceptional problem-solving skills, attention to detail, and effective communication are vital soft skills for this role. These competencies ensure the safe and efficient design of medical devices that meet regulatory requirements and patient safety standards.

What is the difference between Medical Device Systems Engineer vs Medical Device Quality Engineer?

AspectMedical Device Systems EngineerMedical Device Quality Engineer
Required CredentialsBachelor's in Engineering, Systems Engineering certificationsBachelor's in Engineering, Quality Management certifications (e.g., ISO 13485)
Work EnvironmentDesign, develop, and integrate medical device systemsEnsure product quality, compliance, and risk management
Employer & Industry UsageMedical device manufacturers, R&D teamsRegulatory agencies, manufacturing firms, compliance departments
Common Search & ComparisonFocus on system integration and designFocus on quality assurance and compliance

The Medical Device Systems Engineer primarily focuses on designing and integrating medical device systems, ensuring functionality and performance. In contrast, the Medical Device Quality Engineer concentrates on maintaining product quality, regulatory compliance, and risk management. Both roles are essential in the medical device industry but serve different aspects of product development and manufacturing.

More about Medical Device Systems Engineer jobs
Infographic showing various Medical Device Systems Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $127,215 per year, or $61.2 per hour.

Sr. Systems Engineer, Medical Device

Mizuho OSI

Union City, CA โ€ข On-site

$130K - $150K/yr

Full-time

Re-posted yesterday


Job description

About Company

Mizuho OSI is the leader in the markets for specialty surgery and patient positioning. The companyโ€™s portfolio includes specialty surgical tables for procedure-specific approaches that improve patient outcomes in spine and orthopedic surgeries along with disposable and reusable surgical patient care products.

Job Summary

As Systems Engineer you will be part of a small, agile team; responsible for medical device development projects starting from technology exploration, product definition, to guiding integration with software controlled electromechanical systems; ending with product and release testing.

We develop a broad spectrum of products from sterile disposables to complex capital equipment using a customer-centric, collaborative, innovation driven approach. We value ownership, calculated risk-taking, and tolerance for ambiguity as we build future devices and improve existing products.

We are looking for you, if you have: 

  • Curiosity to explore new approaches and innovative solutions.
  • Intellectual discipline to analyze problems and synthesize solutions. 
  • Grit to drive challenging projects to completion in a fast-pace environment.
  • Enjoy working in a diverse, team driven environment.

 

Responsibilities:

  • Create innovative solutions to address user needs in products that differentiate the company in the market.
  • Translate customer needs into requirements and engineering specifications. Document design input & output.
  • Meld technical contributors into a unified team and collaborate to determine best technologies for the product.
  • Develop, manage and maintain design history files and related deliverables.
  • Develop, maintain and execute to plans, milestones, schedules and task lists.
  • Manage and logically organize data to identify and describe problems and assess the suitability and quality of technical solutions.
  • Maintain up-to-date knowledge of medical devices, technologies and regulatory landscape relate to the companyโ€™s products.
  • Perform complaint, failure and risk management activities, develop mitigation and risk control strategies and generate supporting documentation.
  • Perform engineering, integration, verification and validation testing, including protocol development, report generation and regression analysis. 
  • Develop and document processes, methods and tools for product testing and evaluation. 
  • Support cross-functional Design Transfer process to ensure product designs manufacturable & serviceable.
  • Support product sustaining activities including value engineering, reliability improvements, manufacturability improvements, field issues with technical and impact analysis.
  • Manage, prioritize and align work activities with project schedules.
  • Understand, follow and support Mizuho OSIโ€™s internal Quality System policies, procedures and work instructions including but not limited to applicable external regulations (21 Code of Federal Regulations Part 820 Quality System Regulations and applicable International Standards). 
  • At more senior levels you may: 
    1. Share and provide technical expertise and guidance to other engineers and designers.
    2. Lead projects and team as assigned.
    3. Familiarity with Engineering Applications like MatLab, LabView or EA.  

Qualifications & Requirements:

  • Bachelor's Degree in Engineering or related field 5-8 YOE, Masterโ€™s degree 1-3 YOE, PhD 1+ years of experience. 
  • Strong analytical skills and ability to apply engineering principles using logical or scientific thinking to define problems, collect data, establish facts, and draw valid conclusions.  
  • Ability to comprehend an extensive variety of technical instructions in mathematical and/or diagrammatic form and translate that into design requirement and/or performance.
  • Ability to find creative or innovative solutions for design of products.  
  • Solid understanding of systems engineering principles and methods, system modeling and transformation applications.
  • Ability to make and communicate decisions in a timely fashion; to formulate and execute a course of action.
  • Ability to independently manage and prioritize work based on goals and objectives and provide deliverables in alignment with timelines and deadlines. 
  • Ability to adjust to changing timelines and priorities in a fast paced environment.
  • Ability to collaborate cross-functionally and cross-organizationally and respond to the needs of internal customers.
  • Strong interpersonal and communication skills and ability to effectively work in a team.
  • Excellent written & verbal English communication skills and strong presentation skills.
  • Adept use of Office Applications like MS Outlook, Excel, Word, PowerPoint, Visio and Project.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Salary scale $130,000- $150,000 DOE + potential annual bonus + comprehensive benefits package