STERIS is seeking a qualified professional in Regulatory Affairs based in Hobart, Tasmania, to support compliance with Australian and New Zealand regulations. This position involves preparing regulatory submissions and collaborating with product teams to ensure strategy alignment.
The ideal candidate will have 3–5 years of experience in the medical device industry and a strong understanding of regulatory frameworks and ISO standards. Join STERIS to help navigate regulatory landscapes and contribute to global product approval processes.
#J-18808-Ljbffr