- Prepare, review, and submit regulatory
documentation to the Thai FDA for product
registration and variation.
- Manage timelines and deliverables for
regulatory submissions to ensure timely
approvals.
- Monitor and interpret changes in regulatory
requirements and communicate their impacts
to cross-functional teams.
- Ensure that products comply with all local,
national, and international regulations,
guidelines, and standards throughout the
lifecycle.
- Serve as the primary point of contact for
regulatory agencies, facilitating clear
communication and problem-solving during
interactions.
- Develop and execute regulatory strategies
for medical device products, ensuring
alignment with business objectives.
- Always up-to-date on regulatory trends
พฤษภาคม 2562 ถึง กุมภาพันธ์ 2565
Regulatory affairs
Somnotec Co., Ltd.
Bangkok
สำหรับสมาชิกเท่านั้น
- Prepare, review, and submit regulatory
documentation to the Thai FDA for product
registration and variation.
Manage timelines and deliverables for
regulatory submissions to ensure timely
approvals.
- Monitor and interpret changes in regulatory
requirements and communicate their impacts
to cross-functional teams.
- Ensure that products comply with all local,
national, and international regulations,
guidelines, and standards throughout the
lifecycle.
- Serve as the primary point of contact for
regulatory agencies, facilitating clear
communication and problem-solving during
interactions.
- Always up-to-date on regulatory trends.