Steris is seeking a Regulatory Affairs & Quality Specialist in Melbourne, VIC, with 3-5 years of experience in regulatory affairs within the medical device industry. The role involves preparing regulatory submissions, ensuring compliance with Australian regulations, and collaborating across departments to support regulatory policies. Candidates should have strong knowledge of ISO standards, and experience with medical device registration is preferred. The position offers opportunity to work in a fast-paced environment and contribute to the development of innovative healthcare solutions.#J-18808-Ljbffr