Senior Electrical Engineer Sydney 12-month Fixed Term Contract Attractive Salary (negotiable) Are you looking for a Senior Electrical Engineer role in Sydney? Do you have experience of working with medical devices or in another regulated industry? Do you have a passion for staying up to date with the latest advancements in electrical engineering and medical technologies? I’m recruiting for an innovative, medical devices company that’s developing the world’s next generation of implantable device technology. About the Company My client is a leading global healthcare company, established for over a decade, who are looking for a Senior Electrical Engineer to expand their Sydney engineering team. Passionate about improving patients’ lives their technology is leading to a new generation of therapies. The Role You will have strong hands-on technical skills in one or more key electrical engineering domains. 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. You will participate 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. 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 Skills and experience 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 multilayer 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 analogue / mixed-signal ASICs Understanding of frontend analogue 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 Benefits Contribute to the development and enhancement of cutting-edge medical devices that improve lives Thrive in a fast-paced, regulated environment that values your attention to detail and commitment to excellence Collaborate with a talented team of professionals dedicated to delivering world-class products and solutions N.B. You must possess full, unrestricted and ongoing rights to work in Australia to be eligible for this role. (Please ensure this is clearly stated on your CV).