Job Description
<Job Responsibilities> - Prepare and organize documents required for SIPT registration - Translate and submit regulatory documents - Coordinate internal timelines and external consultants - Track submission progress and maintain documentation - Other responsibilities as needed
Job Requirement
<Necessary Skill / Experience > ・Bachelor's degree or higher in clinical medicine, biology, biotechnology, pharmacy and related majors. ・English Business level. ・Minimum of 3 years of experience in manufacturing as Regulatory Affairs Specialist in the medical equipment industry, familiar with Indonesian medical device registration (SIPT) ・Good communication skill, good work ethics, able to multitask <Preferable Skill / Experience> ・Mandarin conversation level or above ・Experienced working in Japanese or Chinese medical device company