APAC Regulatory Affairs Specialist - Medical Devices

A leading global medical device company in Singapore is seeking a Regulatory Affairs Specialist to coordinate product registration and market access in the APAC region. The ideal candidate has at least 2 years of experience in regulatory affairs within the medical device industry, with strong knowledge of relevant regulations. This role emphasizes proactive problem-solving, effective collaboration, and detailed oversight of post-market activities. Interested applicants are encouraged to apply.