ZipRecruiter

Log In

1

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

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 ...

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

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

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 ...

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 ...

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 ...

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 ...

Astrix Inc

Assembly Technician

Santa Rosa, CA · On-site

$22 - $26/hr

This is a great opportunity for someone with medical device, cleanroom, manufacturing, or small ... Support troubleshooting efforts with supervisors, engineers, and technicians. * Participate in Lean ...

Endologix

Quality Control Inspector

Santa Rosa, CA · On-site

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Support continuous improvement efforts by partnering with Manufacturing, Engineering, and Quality ...

Endologix

Quality Control Inspector

Santa Rosa, CA

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Support continuous improvement efforts by partnering with Manufacturing, Engineering, and Quality ...

Endologix

Quality Control Inspector

Santa Rosa, CA

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Support continuous improvement efforts by partnering with Manufacturing, Engineering, and Quality ...

Abbott

Quality Engineer

Santa Rosa, CA · On-site

$78K - $101K/yr

Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow, and learn, care ... Minimum of five to eight years of Quality Assurance experience in a regulated FDA medical device ...

Abbott

Quality Engineer

Santa Rosa, CA · On-site

$78K - $101K/yr

Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow, and learn, care ... Minimum of five to eight years of Quality Assurance experience in a regulated FDA medical device ...

next page

Showing results 1-20

All JobsR&D Engineer Medical Device JobsInternship R&D Engineer Medical Device JobsInternship R&D Engineer Medical Device Jobs in Santa Rosa, CA

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 Jul 23, 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
Sr. Supplier Quality Engineer

Sr. Supplier Quality Engineer

Endologix

Santa Rosa, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 27 days ago

Job description

Overview
Join our Quality team as the Sr. Supplier Quality 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:
We're looking for a Sr. Supplier Quality Engineer to join our Quality team. The Sr. Supplier Quality Engineer (SQE) is responsible for ensuring that purchased materials, components, and services meet defined quality, regulatory, and business requirements. This role partners closely with suppliers and internal cross-functional teams to manage supplier performance, drive continuous improvement, and support product quality throughout the product lifecycle. The Sr. SQE serves as a technical leader and subject matter expert responsible for end-to-end supplier quality strategy, governance, and risk management across the product lifecycle in a regulated medical device environment.
Responsibilities
WHAT YOU'LL DO:
  • Lead supplier identification, qualification, maintenance, and ongoing monitoring activities to ensure suppliers consistently meet quality, reliability, and compliance expectations that ultimately support positive patient outcomes.
  • Own and manage the Approved Supplier List (ASL) and Approved Component List (ACL), ensuring accuracy, transparency, and alignment with quality system requirements.
  • Drive the implementation and assessment of supplier-related change orders, utilizing sound judgment and risk-based decision-making to support continuous advancement and operational excellence.
  • Review and approve supplier changes, deviations, and documentation to ensure compliance with internal procedures, regulatory requirements, and the highest quality standards.
  • Lead supplier Corrective and Preventive Actions (CAPAs) and Supplier Corrective Action Requests (SCARs), conducting thorough root cause investigations and implementing sustainable solutions that strengthen supplier performance.
  • Investigate supplier-related nonconformances and quality issues, partnering with cross-functional stakeholders to implement effective containment, corrective actions, and risk mitigation strategies.
  • Support Material Review Board (MRB) activities, nonconforming material disposition decisions, and failure investigations to ensure timely resolution of issues while maintaining product quality and supply continuity.
  • Own supplier performance governance, including scorecards, business reviews, performance metrics, and escalation processes that promote accountability, transparency, and continuous improvement.
  • Develop, review, and maintain high-quality technical documentation, including procedures, reports, justifications, and quality records, ensuring accuracy, clarity, and regulatory compliance.
  • Collaborate closely with Engineering, Manufacturing, Regulatory Affairs, Supply Chain, Operations, and external suppliers to solve complex challenges, drive innovation, and deliver exceptional results.
  • Lead supplier audits, including preparation, execution, follow-up, and remediation activities, fostering strong supplier partnerships while ensuring adherence to quality and regulatory expectations.
  • Apply project management principles to effectively manage competing priorities, timelines, and deliverables in a dynamic and evolving environment.
  • Champion continuous improvement initiatives by identifying opportunities to enhance supplier quality processes, systems, tools, and performance metrics.
  • Demonstrate initiative, adaptability, and a willingness to challenge the status quo to drive meaningful improvements and advance organizational objectives.
  • Perform other duties as assigned by management in support of departmental and organizational goals.

Qualifications
WHAT YOU'LL BRING:
Education:
  • Bachelor's degree in Engineering, math or related discipline; Master's degree preferred.

Experience:
  • Minimum of 5+ years of experience in Supplier Quality, Quality Engineering, or a related role
  • Experience working within a medical device quality system and applicable regulations (e.g., ISO 13485, FDA QSR).
  • Demonstrated experience with supplier qualification and management, supplier development, and supplier monitoring.
  • Experience in supporting or leading supplier-related change management activities.

Skills/Competencies:
Required:
  • Strong knowledge of ASL and ACL management and supplier lifecycle controls.
  • Demonstrated leadership in:
    • Supplier qualification, development, and risk management programs
    • Process validation strategy (IQ/OQ/PQ/PPQ) and statistical methods
    • Supplier change management and regulatory impact assessments
  • Solid understanding of CAPA methodologies, root cause analysis, and effectiveness checks.
  • Experience leading SCARs and driving prompt, effective supplier corrective actions.
  • Excellent technical writing skills with the ability to produce clear, concise, and compliant documentation.
  • Strong cross-functional collaboration and communication skills.
  • Effective project management skills, including prioritization, planning, and execution.
  • Supplier audit experience.
  • Willingness to travel domestically and internationally for supplier visits and audits.
  • Ability to work independently, manage multiple workstreams, and meet deadlines in a fast-paced environment.

Preferred:
  • Experience with QAD, MasterControl or TrackWise highly desired
  • ISO 13485 Lead Auditor certification is a strong plus.

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 $110,000/yr-$127,500/yr
  • 10% 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:
  • Flexible work arrangements, such as hybrid or remote work for many of our positions
  • 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 & 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.

Apply