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Medical Device Manufacturing Jobs in Santa Rosa, CA

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Develop and optimize detailed manufacturing instructions to ensure scalable, repeatable, and high ...

Principal R&D Engineer

Santa Rosa, CA · On-site

$145 - $167.50/hr

... in medical device manufacturing, development, testing, test plans, test reports, design control regulation and experience with catheter and stents. Skills/Competencies: * Product Development:

... in medical device manufacturing, development, testing, test plans, test reports, design control regulation and experience with catheter and stents. Skills/Competencies: * Product Development:

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Experience in assembly or medical device manufacturing is highly preferred. Essential Job Duties * Support the Production Supervisor by assigning daily work responsibilities to Manufacturing ...

New

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Manufacturing Engineer

Santa Rosa, CA · On-site

$105K - $125K/yr

The Manufacturing Engineer's primary responsibility is to implement and optimize product manufacturing and maintaining compliance with FDA and other medical device standards, while also ensuring that ...

Tooling Engineer III

Santa Rosa, CA · On-site

$86 - $135/hr

Experience within medical device manufacturing. ADA Requirements * Stand, walk, bend, squat, twist, reach or otherwise move frequently * Occasional repetitive motion and grasping * Occasional ...

New

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 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 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 ...

Assembly Technician

Santa Rosa, CA · On-site

$22 - $26/hr

This is a great opportunity for someone with medical device, cleanroom, manufacturing, or small component assembly experience who enjoys hands-on work and attention-to-detail focused environments.

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Develop and optimize detailed manufacturing instructions to ensure scalable, repeatable, and high ...

WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to ... Develop and optimize detailed manufacturing instructions to ensure scalable, repeatable, and high ...

Quality Engineer

Santa Rosa, CA · On-site

$78K - $101K/yr

Minimum of five to eight years of Quality Assurance experience in a regulated FDA medical device manufacturing environment or ISO certified laboratory, with 3-5 years progressively responsible ...

Quality Engineer

Santa Rosa, CA

$78K - $101K/yr

Minimum of five to eight years of Quality Assurance experience in a regulated FDA medical device manufacturing environment or ISO certified laboratory, with 3-5 years progressively responsible ...

Quality Engineer

Santa Rosa, CA · On-site

$78K - $101K/yr

Minimum of five to eight years of Quality Assurance experience in a regulated FDA medical device manufacturing environment or ISO certified laboratory, with 3-5 years progressively responsible ...

Medical device, pharmaceutical, biotechnology, or regulated-manufacturing experience is strongly preferred. * Experience partnering with Manufacturing, Engineering, R&D, Quality, or drug-development ...

Showing results 21-40

Medical Device Manufacturing information

See Santa Rosa, CA salary details

$20

$29

$43

How much do medical device manufacturing jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for medical device manufacturing in Santa Rosa, CA is $29.65, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $34.71 per hour, depending on experience, location, and employer.

What is a medical device manufacturing job?

A Medical Device Manufacturing job involves producing, assembling, and testing medical devices to ensure they meet regulatory and quality standards. Workers in this field may operate machinery, inspect products, and follow strict guidelines to maintain safety and efficiency. Roles can range from machine operators and quality control inspectors to engineers and regulatory compliance specialists. This industry is essential for creating devices like surgical instruments, pacemakers, and diagnostic equipment used in healthcare. Attention to detail, adherence to regulations, and technical skills are key for success in this field.

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

To thrive in Medical Device Manufacturing, you need strong attention to detail, knowledge of quality assurance processes, and an understanding of regulatory standards such as ISO 13485 or FDA requirements. Experience with manufacturing equipment, ERP systems, and specialized tools for assembly and testing is typically required, and certification in areas like Six Sigma or Lean Manufacturing can be advantageous. Effective communication, teamwork, and problem-solving skills help individuals excel in fast-paced, multidisciplinary environments. These skills are vital for maintaining product safety, ensuring regulatory compliance, and meeting production targets in the highly regulated medical device industry.

What career advancement opportunities are available in medical device manufacturing?

Medical Device Manufacturing offers a variety of career advancement paths, allowing employees to move into roles such as production supervisor, quality assurance specialist, or process engineer as they gain experience. Many companies provide on-the-job training, mentorship programs, and support for additional certifications to help employees further develop their technical and leadership skills. Team members who demonstrate strong performance and a commitment to continuous improvement may also transition into management positions or cross-functional roles in research and development, regulatory affairs, or supply chain management. This field values both specialized technical expertise and a proactive approach to professional growth, providing long-term career stability and diverse opportunities.

Is medical device manufacturing a good career?

Medical device manufacturing is a stable career that involves assembling, testing, and quality control of medical equipment, often requiring technical skills and certifications. It offers opportunities for advancement and typically provides a clean, regulated work environment, with demand driven by healthcare industry growth.

What cities near Santa Rosa, CA are hiring for Medical Device Manufacturing jobs?

Cities near Santa Rosa, CA with the most Medical Device Manufacturing job openings:

Infographic showing various Medical Device Manufacturing job openings in Santa Rosa, CA as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $61,676 per year, or $29.7 per hour.

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 3 days ago


Job description

Join our innovative, patient-focused Research & Development team as a Sr. R&D Technician 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. R&D Technician to join our Research & Development team. In this role, you’ll independently execute advanced laboratory and product development activities in support of research and development programs. This role contributes technical expertise, ensures rigorous data collection and documentation, and collaborates cross-functionally to accelerate innovation and drive the successful achievement of Endologix’s product and patient-focused objectives.


WHAT YOU'LL DO:

  • Assemble and refine prototype design concepts with precision and a deep understanding of how each advancement contributes to improved patient outcomes.
  • Develop and optimize detailed manufacturing instructions to ensure scalable, repeatable, and high-quality production processes.
  • Conduct comprehensive bench testing of designs and subcomponents, proactively identifying opportunities to enhance performance, safety, and reliability.
  • Execute and, when appropriate, support development of test protocols in full compliance with regulatory and quality system requirements, demonstrating integrity and accountability in all documentation and practices.
  • Perform troubleshooting of test equipment, fixtures, and instrumentation; coordinate calibration activities to maintain data accuracy and laboratory readiness.
  • Maintain thorough, accurate, and transparent records of experimental activities, ensuring compliance with design controls, regulatory standards, and internal quality systems.
  • Record detailed data, observations, and technical conclusions in laboratory notebooks and electronic systems to support traceability, reproducibility, and audit readiness.
  • Analyze test results, summarize findings, and communicate insights clearly to cross-functional stakeholders to drive informed decision-making.
  • Partner collaboratively with engineers, quality, regulatory, manufacturing, and physician advisors to advance product development initiatives and solve complex technical challenges.
  • Demonstrate curiosity and adaptability by contributing ideas for design improvements, process enhancements, and innovative testing approaches.
  • Take initiative in identifying risks, proposing solutions, and supporting continuous improvement efforts with a bold yet thoughtful approach.
  • Mentor junior technicians and provide technical guidance to support team development and operational excellence.
  • Perform additional responsibilities as assigned, supporting team objectives and advancing departmental and organizational goals.

WHAT YOU'LL BRING:

Education:

  • High school diploma or general education degree (GED); or equivalent combination of education and experience.

Experience:

  • Minimum of three (3) years of hands-on laboratory experience in medical device or a related regulated industry; medical device experience preferred.
  • Working knowledge of medical device development processes, including documentation and record-keeping within a quality system environment.
  • Experience maintaining accurate, detailed technical records to support traceability, compliance, and audit readiness.
  • Familiarity with common device materials, including plastics, metals, and adhesives, and their application in product development.
  • Proficiency with general laboratory and bench test equipment (e.g., tensile testers, microscopes, measurement tools, and related instrumentation).
  • Demonstrated ability to follow test protocols, document results clearly, and support regulatory requirements.

Skills/Competencies:

  • Technical Expertise: Strong hands-on laboratory and bench testing skills, including prototype assembly, test method execution, data collection, and troubleshooting of laboratory equipment and fixtures.
  • Design & Development Support: Working knowledge of product development processes, design controls, and verification/validation activities within a regulated medical device environment.
  • Regulatory & Quality Acumen: Solid understanding of documentation practices, traceability requirements, and compliance standards (e.g., FDA Quality System Regulation, ISO 13485) with a commitment to data integrity and audit readiness.
  • Analytical Thinking: Ability to interpret test data, identify trends, troubleshoot technical issues, and provide clear, actionable feedback to engineering teams.
  • Attention to Detail: High level of accuracy in executing protocols, recording observations, and maintaining laboratory documentation.
  • Problem Solving: Proactively identifies technical challenges and contributes practical, well-reasoned solutions that balance innovation with risk mitigation.
  • Collaboration: Effectively partners with R&D engineers, Quality, Regulatory, Manufacturing, and cross-functional stakeholders to support project milestones and deliver results.
  • Communication Skills: Clearly communicates technical findings verbally and in writing; able to summarize complex data in a concise and understandable format.
  • Adaptability & Initiative: Thrives in a fast-paced development environment; demonstrates curiosity, flexibility, and ownership of assigned projects and deliverables.
  • Mentorship & Leadership: Provides guidance to junior technicians and contributes to a culture of continuous improvement and operational excellence.

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:

  • Pay rate of $33.65/hr-$38.46/hr
  • 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 & 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.