Senior Regulatory Affairs Specialist - Medical Devices (ID: 509296)

Advise others on regulatory and compliance matters
Ensure compliance with regulations
Coordinate regulatory documentation activities
Identify and interpret relevant regulatory guideline
Explain regulations, policies, or procedures
Maintain data in information systems or databases
Evaluate applicable laws and regulations to determine impact on company activities
Provide technical review of data or reports
Train other RA team members on Vietnam regulatory requirements as required

Experience gained in multinational companies, especially in Medical devices is a plus
Delivers Results with Integrity: Meets commitments and produces the right results at the right time. Adheres to moral and ethical principles. Believable and trustworthy. Does what he/she says they are going to do
Initiative: Proactive. Takes action without prompting or direction from others. Constantly strives to improve own and company performance
Minimum 2 years RA experience.
Teamwork/Supporting our Colleagues: Collaborates with co-workers to achieve work group and company goals
Focuses on the Customer: Is dedicated to meeting the needs of internal and external customers

Phụ cấp
Tăng lương
Nghỉ phép năm
Chế độ thưởng
Chế độ bảo hiểm
Phụ cấp thâm niên
Đào tạo
Chăm sóc sức khỏe
Laptop

Cập nhật gần nhất lúc: 2021-04-03 09:20:31