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 We are seeking a Senior Electrical Engineer with strong hands‑on technical skills in one or more key electrical engineering domains to join our Sydney engineering team. This is a technically focused role contributing directly to the design, development, verification, and support of active implantable medical devices and their supporting accessories. Depending on your background, you will take technical ownership in areas such as RF systems, firmware, mixed‑signal ASICs, or PCB design, while working closely with internal teams and external development and manufacturing partners. You will contribute at both component and system level, influencing architecture, requirements, and design decisions, and participating actively in technical reviews throughout the product lifecycle. This role requires engineers who can write high‑quality technical documentation and communicate complex ideas clearly to both technical and non‑technical stakeholders. This is a 12 month, Fixed term contract position Your role will include: Contribute to the design and development of electrical and electronic subsystems for implantable and external medical devices Provide deep technical expertise in one or more of the following areas: Mixed‑signal ASIC development RF system design and compliance Embedded firmware PCB design and layout Develop and review technical requirements, specifications, and design documentation Participate in schematic, layout, firmware, and system‑level design reviews, including designs produced by external partners Assist with debugging, root cause analysis, and issue resolution during development and manufacturing transfer Communicate technical concepts, risks, and trade‑offs effectively to engineers, quality, regulatory, and operations stakeholders Support verification and validation activities, including test method development and analysis of results Collaborate closely with systems engineering, firmware, mechanical, quality, regulatory, and manufacturing teams Ensure designs meet safety, performance, reliability, and regulatory requirements appropriate to medical devices Core Technical Skills (One or More Required) Candidates are expected to demonstrate strong depth in at least one of the following areas: RF and Wireless Systems Design and integration of Bluetooth or other RF systems Antenna integration, coexistence, and EMC considerations Experience supporting RF compliance and regulatory testing PCB Design and Layout Schematic capture and multi‑layer PCB design Layout for mixed‑signal, low‑noise, and RF‑sensitive systems Familiarity with design for manufacturability and test Embedded Firmware Strong embedded programming skills (e.g. C ) Experience developing firmware for low‑power or safety‑critical systems Familiarity with hardware‑software integration and debugging Mixed‑Signal ASIC Development Experience specifying, designing, or supporting analog / mixed‑signal ASICs Understanding of front‑end analog design, data converters, power management, and signal integrity Experience working with ASIC vendors or design houses It’s not essential, but nice if you have: Knowledge of analogue electronics, including SPICE‑based simulation Proficiency using modelling and simulation tools such as LTspice Strong programming fundamentals beyond embedded level (e.g. Python, C#) Knowledge of control systems, digital signal processing (DSP), and neurophysiology Experience with Test Method Validation and FMEA Experience working in quality‑controlled and regulated environments, including familiarity with ISO 13485 and IEC 62304 At Saluda, we challenge boundaries. We innovate and think beyond the conventional. We disrupt. 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.
