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