Senior Verification

Senior Verification & Validation Engineer - Process Transformation Join to apply for the Senior Verification & Validation Engineer - Process Transformation role at Resmed We are seeking a Verification & Validation (V&V) Engineer who thrives at the intersection of engineering rigour and innovation. In this role, you won’t just execute V&V activities—you’ll reimagine how they’re done, applying artificial intelligence and automation to transform processes, reduce complexity, and unlock new levels of efficiency and insight. You’ll play a pivotal role in shaping the future of product verification in a regulated environment, ensuring safety and compliance while driving smarter, faster, and more adaptive workflows. If you’re excited by the challenge of modernising traditional engineering practices, improving patient outcomes and creating meaningful impact, this is the role for you. Key Responsibilities Be a Change Agent: Promote and embed a growth mindset to improve compliance, scalability, and overall V&V effectiveness. Future-Proof Capabilities: Scout, evaluate, and pilot emerging technologies to keep V&V innovative and forward‑looking. Integrate Across Functions: Partner with other functions to implement tools that improve collaboration and system integration. Guide Strategic Decision‑Making: Using data, AI, and automation to deliver insights that optimize test focus, resource allocation, and early detection of risks or design gaps. Own Process Innovation: Identify, design, and implement initiatives that streamline V&V activities, reduce manual effort, and improve accuracy, compliance, and effectiveness. Lead AI‑Driven V&V Transformation: Drive the integration of AI into verification and validation, advancing predictive testing, automation, and data‑driven strategies. Enhance Data & Automation Use: Champion advanced automation and analytics for robust requirements traceability, risk assessment, and defect detection. Regulatory & Audit Leadership: Oversee creation and validation of V&V documentation and justifications for regulatory submissions. Qualifications & Experience Essential Bachelor’s degree in Engineering or Science. 5+ years of experience in Verification & Validation, Systems Engineering, or related functions within a regulated industry, with demonstrated technical leadership in complex projects. Proven track record applying AI and automation to engineering workflows—including predictive analytics, automated decision support, testing automation, or large‑scale data integration. Strong working knowledge of requirements management tools (e.g., DOORS, Jama, Jira) and use of data science environments (e.g., Python, MATLAB, Jupyter). Exceptional analytical and problem‑solving skills with the ability to translate technical insights into strategic recommendations for leadership and cross‑functional teams. Preferred Substantial experience in medical devices or similarly regulated industries. Demonstrated contributions to AI in regulatory, quality, or compliance contexts (e.g., AI‑assisted documentation, automated coverage analysis, predictive risk management). Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive, and inspiring. A culture driven by excellence helps you not only meet your goals but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression and thriving on innovative ideas. If this sounds like the workplace for you, apply now We commit to respond to every applicant. Seniority Level Mid‑Senior level Employment Type Full‑time Job Function Quality Assurance Industries Software Development, IT Services and IT Consulting, and Medical Equipment Manufacturing Location Sydney, New South Wales, Australia #J-18808-Ljbffr