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Internship R&D Engineer Medical Device Jobs in Santa Rosa, CA

Endologix

Principal R&D Engineer

Santa Rosa, CA · On-site

Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our ...

Endologix

Principal R&D Engineer

Santa Rosa, CA

Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our ...

Hillstone Restaurant Group

Host/Hostess

Yountville, CA · On-site

$37.50 - $45.50/hr

Company Description R+D Kitchen in Yountville is currently seeking Maître d' / Greeter candidates ... Medical/dental benefits are available after an introductory period. Part-time and full-time ...

Endologix

Supplier Quality Engineer

Santa Rosa, CA

Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our ...

Endologix

Supplier Quality Engineer

Santa Rosa, CA

Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our ...

Endologix

Supplier Quality Engineer

Santa Rosa, CA · On-site

Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our ...

Hillstone Restaurant Group

Server

Yountville, CA · On-site

$30 - $50/hr

Company Description R+D Kitchen is currently seeking exceptional candidates to join our service ... Medical/dental benefits are available after an introductory period. * Part-time and full-time ...

Hillstone Restaurant Group

Server

Yountville, CA

$30 - $50/hr

R+D Kitchen is currently seeking exceptional candidates to join our service team. We are searching ... Medical/dental benefits are available after an introductory period. * Part-time and full-time ...

Endologix

Sr. R&D Technician

Santa Rosa, CA

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Partner collaboratively with engineers, quality, regulatory, manufacturing, and physician advisors ...

Endologix

Sr. R&D Technician

Santa Rosa, CA · On-site

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Partner collaboratively with engineers, quality, regulatory, manufacturing, and physician advisors ...

Endologix

Sr. R&D Technician

Santa Rosa, CA

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Partner collaboratively with engineers, quality, regulatory, manufacturing, and physician advisors ...

Apple

Vision Health Scientist/Engineer

Bodega Bay, CA

$181K - $318K/yr

... medical device manufacturers Experience in regulated medical products and/or digital health ... in programming for experimental execution, analysis and/or prototyping Pay & Benefits At Apple ...

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Internship R D Engineer Medical Device information

See Santa Rosa, CA salary details

$12

$21

$32

How much do internship r&d engineer medical device jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for internship r&d engineer medical device in Santa Rosa, CA is $21.12, according to ZipRecruiter salary data. Most workers in this role earn between $17.60 and $22.88 per hour, depending on experience, location, and employer.

What does an Internship R&D Engineer in Medical Device do?

An Internship R&D Engineer in Medical Device assists in the research and development of new medical technologies and products. Their responsibilities typically include supporting senior engineers in designing, testing, and improving medical devices, conducting experiments, collecting and analyzing data, and preparing technical documentation. Interns also learn about regulatory standards and industry best practices while working as part of a multidisciplinary team. This role is ideal for students or recent graduates looking to gain hands-on experience in medical device innovation.

What are the key skills and qualifications needed to thrive as an Internship R&D Engineer in Medical Devices, and why are they important?

To thrive as an Internship R&D Engineer in Medical Devices, you generally need a background in biomedical engineering or a related field, with strong analytical and problem-solving abilities. Familiarity with CAD software, lab equipment, and basic knowledge of regulatory standards like ISO 13485 is important, and prior internships or relevant coursework can be advantageous. Attention to detail, effective communication, and collaborative teamwork skills help you contribute meaningfully to projects and navigate cross-functional environments. These skills ensure you can support innovative product development while adhering to strict safety and quality standards in the medical device industry.

What is the difference between Internship R&D Engineer Medical Device vs R&D Engineer Medical Device?

AspectInternship R&D Engineer Medical DeviceR&D Engineer Medical Device
QualificationsEnrolled in or recent graduate of engineering/biomedical programsBachelor's or Master's in engineering/biomedical fields
Work EnvironmentInternship programs, entry-level projects, supervised tasksFull-time, independent project work, team collaboration
ResponsibilitiesAssisting in research, testing, and documentationDesign, develop, and improve medical device products
Industry UsageCommonly used for training and entry-level experienceCore role in product development and innovation

In summary, the Internship R&D Engineer Medical Device is an entry-level position designed for students or recent graduates gaining initial industry experience. The R&D Engineer Medical Device is a full-time professional role with greater responsibilities in product development and innovation within the medical device industry.

What types of projects or tasks can an Internship R&D Engineer expect to work on in the medical device industry?

As an Internship R&D Engineer in the medical device industry, you can expect to be involved in a variety of projects such as prototyping new device concepts, conducting laboratory experiments, performing data analysis, and supporting design verification and validation activities. Interns often collaborate closely with multidisciplinary teams, including senior engineers, regulatory specialists, and clinicians, to help solve real-world problems and improve patient outcomes. This hands-on experience provides valuable insight into the product development lifecycle and offers opportunities to contribute to meaningful projects that can enhance your technical and professional skills.
What cities near Santa Rosa, CA are hiring for Internship R&D Engineer Medical Device jobs? Cities near Santa Rosa, CA with the most Internship R&D Engineer Medical Device job openings:
Internship R D Engineer Medical Device jobs near you
Infographic showing various Internship R&D Engineer Medical Device job openings in Santa Rosa, CA as of June 2026, with employment types broken down into 50% Full Time, 17% Temporary, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $43,924 per year, or $21.1 per hour.
Principal R&D Engineer

Principal R&D Engineer

Endologix

Santa Rosa, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago

Job description

Overview
Join our innovative, mission-driven R&D team as a Staff R&D Engineer at Endologix!
WHO WE ARE:
Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician training-supported by industry-leading clinical evidence. At Endologix, we're driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health.
What sets us apart is not just our technology, but our culture. At Endologix, we foster a forward-thinking, mission-driven environment where every team member plays a vital role in advancing patient care. Our core values guide how we operate. As for our people? We empower them with the tools, trust, and continuous learning they need to grow. If you're passionate about making a meaningful difference in healthcare, you'll find purpose and belonging here.
Our Core Values are the guiding principles informing our choices and actions, because our customers and patients depend on us:
  • Patient Outcomes Drive Us: We improve lives with every advancement we deliver.
  • Integrity Defines Us: We do what's right, stay transparent, prioritize quality, and own our actions.
  • Innovation Advances Us: We stay curious, adaptable, and push boundaries.
  • Boldness Propels Us: We take smart risks and are unafraid in our pursuit of excellence.
  • Collaboration Unites Us: We partner across teams and with physicians to drive exceptional results.

ABOUT THE ROLE:
The Principal R&D Engineer is responsible for providing subject matter expertise and engineering leadership in the development of Aortic and Peripheral Vascular technologies including enhanced and new stent graft and catheter-based delivery systems to ensure achievement of Endologix goals and objectives.
Responsibilities
WHAT YOU'LL DO:
  • Drive technology and product development from early concept through commercialization, maintaining a strong focus on delivering meaningful, real-world impact.
  • Lead the design and execution of rigorous testing strategies, including experimental design, data analysis, and clear scientific reporting to support confident decision-making.
  • Partner closely with R&D, Manufacturing, Regulatory, and Quality teams to investigate and resolve technical challenges, ensuring timely and effective solutions.
  • Provide technical leadership with clear, professional communication across all levels, while ensuring all work is accurately documented in compliance with GMP and applicable procedures.
  • Collaborate with engineers, machinists, and QA to develop innovative designs for new products, enhancements, and tooling solutions.
  • Plan and execute testing activities to confirm designs meet defined specifications, performance expectations, and quality standards.
  • Evaluate failure modes and conduct detailed technical risk analyses to strengthen product reliability and performance.
  • Maintain thorough and compliant documentation in alignment with the company's quality system and regulatory expectations.
  • Guide and support technicians and, when needed, lead cross-functional teams to achieve shared project goals.
  • Lead and contribute to cross-functional project teams, effectively managing resources and priorities to deliver successful outcomes.
  • Proactively identify hazards and mitigate risks using structured approaches such as Design and Process FMEA.
  • Manage complex projects across multiple disciplines, defining scope, setting objectives, and applying structured problem-solving to ensure efficient execution.
  • Apply thoughtful judgment and calculated risk-taking to overcome technical challenges and drive projects forward.
  • Oversee project budgets responsibly, ensuring effective use of resources while meeting project objectives.
  • Collaborate with New Product Development teams to support component qualification and ensure readiness for production.
  • Take on additional responsibilities as needed to support team success and evolving organizational priorities.

Qualifications
WHAT YOU'LL BRING:
Education:
  • Bachelor's degree in Mechanical Engineering, Bioengineering from a four-year college or university; or related major in Life Sciences preferred

Experience:
  • 11+ years of relevant experience with a Bachelor's degree, or 9+ years of relevant experience with a Master's degree, or 6+ years of relevant experience with a PhD in medical device manufacturing, development, testing, test plans, test reports, design control regulation and experience with catheter and stents.

Skills/Competencies:
  • Product Development: Expertise in driving product and technology development from concept through commercialization.
  • Testing & Validation: Ability to design, plan, and execute rigorous test plans, including experimental design, data analysis, and scientific reporting.
  • Engineering Design: Proficiency in collaborating with engineers, machinists, and QA to develop product designs, revisions, and tools.
  • Risk Analysis: Skilled in assessing failure modes, conducting technical risk analysis, and mitigating risks through Design and Process FMEA.
  • Quality Compliance: Knowledge of GMP, SOPs, and quality system documentation requirements.
  • Team Leadership: Ability to lead and supervise cross-functional teams, including technicians and professional staff.
  • Project Planning: Skilled in organizing projects across multiple disciplines, defining scope, and problem-solving methods.
  • Cross-functional Collaboration: Effective at coordinating with R&D, Manufacturing, Regulatory, Quality, and NPD teams.
  • Decision Making & Risk Taking: Strong decision-making skills, particularly under technical uncertainty or critical issue resolution.
  • Communication: Professional and effective interaction with senior management, peers, team members, customers, and other departments.
  • Collaboration: Demonstrated ability to work collaboratively across various functions and teams.
  • Documentation: Meticulous in documenting technical work to meet company and regulatory standards.
  • Problem Solving: Analytical mindset with the capability to identify hazards and develop mitigation strategies.
  • Adaptability: Flexibility to manage multiple projects and adjust priorities as needed.

WHAT WE OFFER:
At Endologix, we know that great work starts with great people - and people do their best when they feel valued and supported. That's why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You'll be part of a team that's making a real impact on patients' lives. When you join us, you're not just taking a job, you're building a meaningful career with a team that's invested in your success.
The compensation package includes:
  • Base salary of $145,000-$167,500/year
  • Discretionary bonus
  • Equity participation as approved by Board of Directors (4-year vesting schedule)
  • Comprehensive health, dental, and vision insurance plans
  • Flexible Health Savings Accounts (HSAs) and/or Flexible Spending Accounts (FSAs)
  • Generous paid time off (vacation, sick leave, holidays, and flexible time off that is available for Exempt employees)
  • 401(k) retirement plan with company match

Plus:
  • Employee wellness initiatives, mental health resources, and Employee Assistance Program (EAP)
  • Employee recognition programs and awards
  • Commuter benefits or transportation stipends

OUR COMMITMENT TO EQUAL OPPORTUNITY AND VETERAN INCLUSION:
Endologix LLC is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. As a federal contractor, Endologix LLC is committed to taking affirmative action to recruit, employ, and advance in employment qualified individuals with disabilities and protected veterans.

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