

SUE HUNTER
Regulatory Affairs Director
Abbott Medical
Sue Hunter has been involved in medical device regulatory affairs since joining an orthopaedic company, later to become Zimmer Biomet, in 2010. Sue started her professional life as a veterinary surgeon and has previous experience in varied roles including animal health sales and marketing, as well as regulatory, quality and reimbursement roles in the medical device industry. She is currently Regulatory Affairs Director for Abbott Medical, responsible for ANZ and Canada. The Abbott Medical portfolio includes cardiac arrhythmia and heart failure products, implantable neuromodulation devices targeting pain and movement disorders, as well as coronary and endovascular stents and cardiac valve replacement products.