Demo

Senior Design Quality Engineer - Software

Asensus Surgical
Raleigh, NC Full Time
POSTED ON 2/16/2025
AVAILABLE BEFORE 5/14/2025

Who We Are

At Asensus, we are digitizing the interface between the surgeon and patient to pioneer a new era of Performance-Guided Surgery by unlocking the Clinical Intelligence to enable consistently superior outcomes and a new standard of surgery. Our employees are especially passionate about the work they do and thrive in a collaborative environment that fosters creative solutions to complex problems. The work is challenging, but everyone comes to Asensus looking for a fulfilling career, and that's exactly what they find.

The Role

The role will be part of the Design and Operations Quality team team, which is part of the Global Quality team.

This role will be responsible for conducting activities associated with product development processes at Asensus globally from a Quality perspective, to provide a compliant, safe and effective product that meets customer needs, focused on Software. Activities include generation and management of SOP's, generation and review of documentation, audits, participation in process improvement programs, supporting the product development teams ensuring the quality objectives are understood and achieved. The Design Quality Engineer - Software shall ensure that software systems used in development, manufacturing and as part of medical devices are established according to requirements.

What You'll Do

  • Conducts SW Design quality activities supporting global product development; assists in the development of design concepts, prototypes and product specifications as part of the development team
  • Provides expertise and guidance to Software design verification and validation activities including definition and qualification of test methods, acceptance criteria and statistical principles. Assists in writing and reviewing protocols, reports, work instructions, and SOPs to support product and process development. Ensure compliance to IEC 62304.
  • Defines and develops SW risk management activities including creation and maintenance of risk management files
  • Drives improvements to QMS as a result of quality events, audits or regulatory changes to ensure compliance with FDA 21 CFR 820, ISO 13485, and adoption of best practices.
  • Ensures compliance with Asensus quality and regulatory policies, procedures, and practices through appropriate communication, training, and education of sound quality assurance and regulatory principles.
  • Contributes to develop and maintain processes and controls to ensure software safety, effectiveness and cybersecurity.
  • Builds and maintains a strong and fruitful relationship with SW and global R&D for Design quality aspects
  • Contributes to cross-functional activities that support business goals
  • Support EFT management as assigned
  • Supports internal audits and CAPA activities as applicable
  • All Other Essential Duties as directed

What You Bring

  • Bachelor's degree in engineering discipline. Master's degree in engineering discipline preferred.
  • 5 years in a quality engineering role in the Medical Device field or highly regulated industry
  • Minimum 3 years in a quality role with focus on Software
  • Knowledge of and experience in IEC 62304 and experience with software design and validation for medical devices
  • Knowledge of the standards related to medical devices, including ISO 13485, 21 CFR Part 820 and ISO 14971
  • Understanding of design control, disciplined product development processes, regulatory, and quality requirements.
  • ISO 13485 inspections and FDA inspections experience preferred
  • Soft Skills

  • Strong ability to problem solve and manage workload
  • Self-starter with the ability to work towards goals with little day-to-day supervision
  • Solid understanding of approaches to work breakdown, prioritization, and problem solving
  • Must be able to work well in teams cross functionally and influence teams
  • Must be comfortable presenting and explaining data / details
  • Strong ability to understand technical aspects of the product and communicate it with the relevant stakeholders
  • Optional Skills, Experience, and Qualifications

  • ASQ Certification as Certified Quality Engineer or Software Quality Engineer preferred
  • Experience in Human Factors / Usability Engineering for Medical Devices is a plus
  • Experience with CAPA's and Internal Audits is a plus
  • Experience with and knowledge of specific standards is a plus :
  • IEC 60601
  • IEC 80601-2-77
  • IEC 81001-5-1
  • What We Offer

  • A culture-driven environment to achieve our mission and deliver remarkable results
  • Coworkers committed to collaboration and winning the right way
  • Quality products that improve the lives of our customers and patients
  • Ability to discover your strengths, follow your passion and find your own rewarding career
  • Flexible, engaging work environment
  • Competitive benefits package
  • DEI Statement

    At Asensus, we believe in contributing to a society that welcomes diverse voices and values differences in lived experiences, culture, religion, age, gender identity, sexual orientation, race, ethnicity, and neurodiversity. We are committed to ensuring this same environment for our employees - a culture where individuals feel safe, heard, and respected. We celebrate the uniqueness of our global workforce and know that only through inclusion, ongoing learning, and partnership can we succeed. Together we are all stronger.

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