Job Description:
Job Description: Bioinstrumentation Development Engineer – Engineering & Manufacturing Job Industry, Hobart
The Bioinstrumentation Development Engineer in Hobart plays a vital role in designing, developing, and testing electronic and electromechanical devices used in biomedical applications. This role focuses on integrating sensors, actuators, and embedded electronics into systems that monitor or interact with biological functions. Working within multidisciplinary teams, the engineer contributes to innovations in diagnostics, patient monitoring, therapeutic devices, and laboratory instruments.
Key responsibilities include translating biomedical requirements into functional hardware and embedded software systems. The engineer designs circuits, prototypes devices, and conducts thorough validation of performance under biological conditions. They also optimise signal acquisition, filtering, and processing to ensure accurate measurement of physiological parameters such as ECG, EMG, blood pressure, and neural activity.
The role involves selecting suitable biosensors, microcontrollers, and communication modules while ensuring compliance with medical standards and electromagnetic compatibility regulations. The engineer collaborates closely with biologists, clinicians, and manufacturing teams to refine product design for reliability, safety, and usability.
In Hobart’s growing biomedical technology sector, the engineer contributes to research-oriented projects and commercial medical device development. This includes working on wearable health devices, implantable systems, point-of-care diagnostic tools, and clinical testing platforms. The position is instrumental in bringing healthcare innovations from concept to reality through rigorous engineering processes.
Job Requirement:
Job Requirements: Bioinstrumentation Development Engineer – Engineering & Manufacturing Job Industry, Hobart
The role requires a strong understanding of electronics design, embedded systems, and signal processing, especially as they apply to biological signals. Proficiency in circuit simulation, PCB layout, and embedded C/C++ programming is necessary for developing reliable instrumentation used in sensitive biomedical environments.
Candidates must be capable of working with low-noise analog front-end circuitry, data acquisition systems, and bio-signal amplification. Familiarity with instrumentation amplifiers, A/D converters, and isolation techniques is essential to ensure signal integrity and patient safety. Hands-on experience with development tools such as MATLAB, LabVIEW, and microcontroller IDEs is highly beneficial.
The engineer must understand biomedical regulations and standards such as IEC 60601, ISO 13485, and risk management processes relevant to medical device development. The ability to document design specifications, verification plans, and traceability matrices is essential for regulatory submissions and quality audits.
Excellent problem-solving skills are required for addressing technical challenges in bio-signal accuracy, device miniaturisation, power management, and wireless communication. Collaboration with cross-functional teams, including biologists, software engineers, and regulatory consultants, is vital to ensure device performance and clinical relevance.
Adaptability, precision, and a commitment to innovation are key attributes for this role. The engineer should be detail-oriented and able to manage multiple development cycles, contributing to safe, effective, and technologically advanced solutions for patient care and medical research.
