Posted: 28/04/2026
Closing Date: 15/05/2026
Job Type: Permanent - Full Time
Location: Sydney HQ
Job Category: Research & Product Development
The Opportunity
At Nanosonics, we improve the safety of patients and healthcare professionals worldwide through innovative infection prevention technologies. We're looking for a Senior V&V Engineer to play a critical role in ensuring our products meet the highest standards of quality, performance, and regulatory compliance.
Reporting to the V&V Manager, you will lead and coordinate verification and validation activities across the product development lifecycle. You'll bring technical expertise, analytical thinking, and a hands‐on approach to testing, prototyping, and problem‐solving in a highly collaborative R&D environment.
Key Responsibilities
* Partner with the V&V Manager to define and deliver verification and validation strategies across the product lifecycle
* Plan, coordinate, and execute testing activities across multiple disciplines, ensuring timely delivery and clear progress reporting
* Drive improvements in test efficiency, repeatability, and automation, including development of production test systems
* Conduct prototype testing to identify critical parameters, design sensitivities, and performance limits
* Develop and implement innovative test methodologies, providing data‐driven insights to inform design decisions and reduce iteration cycles
* Lead root cause and failure analysis to resolve issues and strengthen product robustness
* Develop and execute V&V protocols and reports, maintaining clear traceability to system requirements
* Review requirements for completeness, clarity, and testability, and evaluate system performance, reliability, and compliance
* Lead system and integration testing, and coordinate with external test houses to support certification activities
What You'll bring
* You're a detail‐oriented engineer who thrives in complex, regulated environments and enjoys solving real‐world problems through data and experimentation.
* 5–10 years in verification & validation, ideally within medical devices
* Strong understanding of the product development lifecycle
* Experience working within ISO 13485 or similar quality management systems
* Proven ability to manage multiple priorities and deliver under pressure
* Excellent communication and stakeholder engagement skills
* Bachelor's degree in Biomedical, Mechanical, Mechatronics, Electrical Engineering, or similar
Why Join Us?
* Work on meaningful technology that improves patient safety globally
* Be part of a collaborative, high‐performing R&D team
* Contribute to innovative products in a growing ASX‐listed company
* Opportunities for growth, impact, and continuous learning
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