Associate (Junior) Verification Engineer - Fixed Term

About Saluda Medical Founded in 2013, Saluda Medical is dedicated to transforming patients' lives with disruptive neuromodulation solutions. As leaders in the field, we have achieved exceptional pain management results through more than a decade of advanced research, development, and clinical experience. We are a global healthcare company redefining Spinal Cord Stimulation (SCS) therapy at the intersection of automated algorithms, real‑time diagnostics, and groundbreaking clinical evidence. Our advanced neuromodulation systems for the next generation of implantable stimulation devices are distinguished by Dose‑Control Technology via measurement of physiological response. What We’re Looking For… This role plays a critical role in ensuring the safety, reliability, and performance of our medical devices through rigorous design verification testing. Reporting to the DVT Lead, you will collaborate across multidisciplinary teams to execute test protocols, analyze results, and contribute to continuous improvement initiatives. This is a 6‑month Fixed Term contract position. Your role will include: You will be responsible for the planning, execution, and documentation of design verification activities, including: Managing and maintaining the DVT lab environment, equipment, and documentation systems Developing and executing verification protocols in compliance with regulatory standards (e.g., ISO 13485, FDA QSR) Performing mechanical, electrical, and systems testing on devices and components Producing high‑quality documentation including test reports, data analysis, and traceability matrices Supporting root cause analysis and corrective actions for test failures Ensuring adherence to Good Documentation Practices (GDP) and WH&S requirements Collaborating with Product Development, Quality, and Regulatory teams to ensure test coverage and compliance Identifying and implementing process improvements in test methods and lab operations Follow established documentation structure to ensure consistency of format, style, quality, clarity, and accuracy. Performing all work duties in a manner that ensures the health and safety of all employees. Contribution to cross‑functional project teams and product development milestones About you At least 2 years’ experience in the design, development and verification of mechanical/electrical components and sub‑assemblies. A bachelor’s degree in Biomedical, Mechatronic, Electrical or Mechanical Engineering or equivalent. Attention to detail and desire to develop knowledge of product development environment. Ability to communicate and collaborate with subject matter experts in various disciplines. Logical mindset, ability to work with numbers, basic understanding of product inspections and eagerness to learn more about product testing. Familiarity with Microsoft Office (Word, Excel). Ability to read electrical schematics and debug electrical issues. Ability to read mechanical drawings. Experience using electrical and mechanical lab equipment including oscilloscopes, power supplies, multimeters, force gauges, etc. It’s not essential, but nice if you have: Experience in the medical device field or a similar highly regulated business environment. Experience managing equipment used in an engineering lab. Familiarity with Altium/(PCBA design sw) Familiarity with Solidworks (CAD design sw) Familiarity with Python based scripting 3D printing experience Are you Ready to Join? If you would like to be part of our team developing the world's next generation of implantable device technology, contribute to making an impact on patient care, then this is the opportunity for you Please APPLY NOW Applications will only be considered from candidates with the appropriate approval to work in Australia, no visa or sponsorship is available for this role. All eligible candidates are invited to apply. We respectfully ask for no agency approaches. #J-18808-Ljbffr