STERIS is seeking a Regulatory Affairs qualified to support compliance with Australian and New Zealand regulations.
Responsibilities
Prepare regulatory submissions, collaborate with product teams on strategy, and ensure ISO quality systems are maintained.
Qualifications
3–5 years of experience in the medical device industry, strong knowledge of regulatory frameworks, fluency in English, and familiarity with ISO standards.
Join STERIS to help navigate regulatory landscapes and contribute to global product approval processes. #J-*****-Ljbffr
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