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Endologix

Medical devices for durable vascular repair

Senior Research and Development Technician

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeSanta Rosa, CA, USA$33.65 - $38.46 /hrIn-person

About the Job

Requirements

  • High school diploma or general education degree (GED), or an equivalent combination of education and experience.
  • At least three years of hands-on laboratory experience in the medical device or a related regulated industry; medical device experience is 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 applications in product development.
  • Proficiency with general laboratory and bench test equipment, such as tensile testers, microscopes, measurement tools, and related instrumentation.
  • Ability to follow test protocols, document results clearly, and support regulatory requirements.
  • Hands-on laboratory and bench testing skills, including prototype assembly, test method execution, data collection, and troubleshooting laboratory equipment and fixtures.
  • Working knowledge of product development processes, design controls, and verification and validation activities within a regulated medical device environment.
  • Understanding of documentation practices, traceability requirements, and compliance standards, including FDA Quality System Regulation and ISO 13485.
  • Ability to interpret test data, identify trends, troubleshoot technical issues, and provide clear, actionable feedback to engineering teams.
  • Accuracy in executing protocols, recording observations, and maintaining laboratory documentation.
  • Ability to identify technical challenges and contribute practical solutions that balance innovation with risk mitigation.
  • Ability to partner with R&D engineers, Quality, Regulatory, Manufacturing, and cross-functional stakeholders to support project milestones and deliver results.
  • Ability to communicate technical findings verbally and in writing, and summarize complex data concisely and understandably.
  • Ability to work in a fast-paced development environment and take ownership of assigned projects and deliverables.

Responsibilities

  • Assemble and refine prototype design concepts.
  • Develop and optimize detailed manufacturing instructions to support scalable, repeatable, and high-quality production processes.
  • Conduct bench testing of designs and subcomponents, identifying opportunities to improve performance, safety, and reliability.
  • Execute test protocols and, when appropriate, support their development in compliance with regulatory and quality system requirements.
  • Troubleshoot test equipment, fixtures, and instrumentation, and coordinate calibration activities to maintain data accuracy and laboratory readiness.
  • Maintain accurate records of experimental activities in compliance with design controls, regulatory standards, and internal quality systems.
  • Record 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 to cross-functional stakeholders.
  • Collaborate with engineers, quality, regulatory, manufacturing, and physician advisors to advance product development initiatives and solve technical challenges.
  • Contribute ideas for design improvements, process enhancements, and innovative testing approaches.
  • Identify risks, propose solutions, and support continuous improvement efforts.
  • Mentor junior technicians and provide technical guidance.
  • Perform additional assigned responsibilities in support of team and departmental objectives.

Desired Qualifications

  • Medical device industry experience.

About the Company

Endologix

Medical devices for durable vascular repair

Endologix develops vascular medical devices to treat abdominal aortic aneurysms (AAA) and peripheral artery disease (PAD). It sells advanced graft systems used inside blood vessels to repair weakened arteries and improve blood flow. Its products, such as AFX, Ovation, and ALTO, are designed to fit and work with a patient's own artery anatomy to provide durable, stable repairs and preserve the natural bifurcation of the vessels. The company differentiates itself through a focus on preserving native vascular anatomy, offering personalized repair options, and pursuing ongoing clinical excellence and product refinement. Its goal is to help healthcare professionals deliver better outcomes for patients with vascular conditions by providing reliable, long-lasting devices that address unmet needs in vascular care.

Company size
501-1,000
Company stage
IPO
Headquarters
Santa Rosa, CA
Founded
1992

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