Endologix

Principal R&D Engineer

Endologix • $120K — $150K *
Santa Rosa, CA 95403In-Person
Pharmaceuticals & Biotech
11 - 15 years of experience
2 months ago
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Mechanical Engineering, Bioengineering or related Life Sciences major
  • 11+ years experience with Bachelor's, 9+ years with Master's, or 6+ years with PhD in medical device development
  • Expertise in product and technology development from concept through commercialization
  • Skilled in testing, validation, and design control regulation
  • Strong knowledge of GMP and quality documentation standards
  • Experience leading cross-functional teams and collaborating effectively
  • Proficient in risk analysis and failure mode assessments

Responsibilities

  • Drive product development from early concept through commercialization with real-world impact
  • Lead the design and execution of testing strategies and clear scientific reporting
  • Partner with R&D, Manufacturing, Regulatory, and Quality to resolve technical challenges
  • Provide technical leadership and ensure compliant documentation
  • Collaborate with teams to develop innovative designs and tooling solutions
  • Evaluate failure modes and conduct technical risk analyses
  • Guide technicians and lead cross-functional project teams to achieve goals

Benefits

  • Competitive pay along with performance-based bonuses and equity options
  • Comprehensive health, dental, and vision insurance
  • Flexible Health Savings Accounts and/or Flexible Spending Accounts
  • Generous paid time off and flexible time off policies
  • 401(k) retirement plan with company match
  • Employee wellness initiatives and mental health resources
  • Employee recognition programs and commuter benefits
Full Job Description
Overview

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:
  • Competitive Base salary
  • 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

About Endologix

Endologix, Inc. develops, manufactures, markets, and sells medical devices for the treatment of abdominal aortic aneurysms in the United States, the United Kingdom, Japan, Germany, Spain, Italy, and France. It offers minimally-invasive endovascular aneurysm repair (EVAR) products, including AFX (Anatomical Fixation) endovascular AAA system, which is a minimally invasive delivery system; VELA Proximal Endograft, which is designed for the treatment of proximal aortic neck anatomies with AFX; and the Ovation abdominal stent graft system. The company also provides endovascular sealing (EVAS) product, the Nellix EVAS system for the treatment of infrarenal abdominal aortic aneurysms; and accessories for use in the treatment of AAA, including compatible guidewires, inflation devices, and snares. It sells its products through direct sales force, distribution agreements, and other arrangements to hospitals and medical centers. The company was founded in 1992 and is headquartered in Irvine, California.
Learn more about Endologix
Size
528 employees
Market Cap
$4
Industry
Healthcare
Founded
1992
5 Year Trend
-60%
NASDAQ
ELGX
* Ladders Estimates

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