Global Medical Device Regulatory Specialist

A leading medical device company in New South Wales is seeking an experienced Regulatory Affairs Specialist. The role involves developing regulatory strategies, preparing submissions, and ensuring compliance with regulations in diverse markets including the EU, Australia, and the US. Candidates should have a Bachelor's degree in a relevant field and possess strong communication skills. Joining a dedicated team, you will contribute to the innovative world-class products aimed at transforming neurological emergency diagnosis and treatment.