เกี่ยวกับตำแหน่งนี้
The Assistant Manager - Regulatory Affairs will be responsible for the registration/market access process, quality management system establishment and maintenance, and customer satisfaction.
หน้าที่รับผิดชอบ
• Responsible for registration/market access process
• Create, compile, and manage regulatory filings
• Maintain Dealer Licenses
• Establish and maintain GDPMD Quality Management System
• Participate in post market surveillance activities
• Monitor and report regulation updates and RA registration status
คุณสมบัติ
• Bachelor’s Degree in pharmacy, medical device, biology, or related field
• 4 - 7 years experience in regulatory affairs for medical devices
• Proficient in English & local language
• Good knowledge of Microsoft Office
• Travelling Requirements: As required
สิทธิประโยชน์
30,000 - 50,000 THB per month