Sr Staff Reliability Engineer

Aviso, LLC

Sr Staff Reliability Engineer

Fremont, CA
Full Time
Paid
  • Responsibilities

    Position Overview

    An innovative and growing medical technology company is seeking a Reliability Quality Engineer to ensure the product reliability and quality of a complex, next-generation medical device ecosystem. In this permanent, full-time role, you will develop and execute product reliability test plans and verification procedures based on design specifications. You will partner closely with R&D, Systems Engineering, Manufacturing, and Quality teams to ensure highly reliable, advanced medical systems are designed, verified, and launched successfully.

    What Your Day-to-Day Will Involve

    Lead System-Level Reliability: Drive reliability strategy and testing for complex electromechanical medical devices, ensuring robust product performance across the design lifecycle.

    Apply Advanced Methodologies: Utilize reliability engineering tools such as Weibull analysis, Reliability Modeling, Fault Tree Analysis, Accelerated Life Testing (ALT), HALT/HASS, and structured root cause analysis to drive data-based design decisions.

    Define Requirements: Establish reliability requirements, reliability growth plans, and demonstration strategies for NPI (New Product Introduction) programs and sustaining design changes; devise test protocols and author comprehensive test reports.

    Execute Testing: Design and execute reliability test protocols for mechanical, electrical, environmental, and software-driven subsystems across system, subsystem, and component levels.

    Cross-Functional Partnership: Partner with Systems Engineering and R&D to ensure proper linkage between design requirements, risk management, reliability verification, and validation activities.

    Analyze Field Data: Drive reliability insights through the analysis of field data, complaint trends, and nonconformance data to support product improvements and risk mitigation.

    Collaborate on Robustness: Work alongside R&D, Manufacturing Engineering, Supplier Quality, Regulatory Affairs, and Failure Analysis teams to resolve reliability issues.

    Build Infrastructure: Develop and implement reliability testing infrastructure, including custom fixtures and automated test setups.

    Champion Culture: Foster a data-driven reliability culture by mentoring engineers and promoting best practices in reliability engineering and statistical analysis.

    Maintain Compliance: Ensure alignment with ISO 13485, FDA Quality System Regulations (21 CFR 820), and applicable regulatory standards.

    EHS Alignment: Understand and adhere to standard corporate Environmental Health and Safety (EHS) policies.

    Qualifications (Required)

    Education: Bachelor’s or Master’s degree in Engineering (e.g., Biomedical, Electrical, or Mechanical).

    Experience: 5+ years of experience in the medical device industry (or an equivalent regulated industry) demonstrating dedicated reliability expertise.

    Technical Domain: Strong background working with Capital Equipment, complex electromechanical systems, and embedded software devices.

    Testing Expertise: Proven experience defining and executing Accelerated Life Testing (ALT), HALT/HASS, and reliability verification strategies.

    Predictive Analysis: Experience performing reliability prediction analyses using established industry standards such as MIL-HDBK-217, Telcordia, and FIDES.

    Software Skills: Ability to maintain automated testing frameworks using Python and C++ to execute tests.

    Soft Skills: Strong analytical, problem-solving, and statistical analysis skills, with the communication clarity needed to influence cross-functional engineering teams.

    Qualifications (Preferred)

    ASQ CQE (Certified Quality Engineer) or CRE (Certified Reliability Engineer) certification.

    Basic machine tool and manufacturing experience.