**KEY RESPOSIBILITIES** • Responsible for new product registration and variation • Keeping up-to-date with changes in regulatory legislation and guidelines • Implement regulatory strategy for medical device license renewal and maintenance • RA Documents & records control according to QMS **JOB QUALIFICATION** • Bachelor's degree, especially in science (biomedical engineering, biology, chemistry, microbiology and etc.) is preferred. • Minimum 2 years experience in the medical device and or related field, especially in RA is highly preferred. • Positive attitude • Good interpersonal Skills and Team Player