Job Description
Assistant Regulatory Affairs
Prepared, submitted, and monitored product registrations for medical device with Thai authorities (e.g., Thai FDA and others if relevant). Communicate effectively with internal/external stakeholders involved in the product registration process to ensure timely approval. Stay up-to-date with relevant legislation, standards, and registration processes in target countries to support RA manager in product registration strategy and planning. Ensure regulatory compliance throughout the entire product development process. Qualifications:
Bachelor’s degree with a major in Science or related field. Experience in the Medical Device industry is preferred. At least 3 year experience in the medical device industry, especially in regulatory or any related industry. Fluent in English