Regulatory Affairs Specialist. International Project.

Are you looking for the next challenge in your career?

Would you like to be part of an international, highly qualified team working on a strategic medical device market entry project in China ?

We are currently supporting a new project related to the Chinese market entry of a Continuous Glucose Monitoring (CGM) device , with a strong focus on regulatory activities and NMPA approval processes.

Your benefits:

• Competitive salary
• Long-term secure contract
• International project with the latest technologies
• Possibility of working remotely with a flexible schedule
• Integration in a highly qualified team of professionals
• Travel abroad with your project
• Specialized training and continuous professional development
• Social benefits and a flexible compensation plan

Responsibilities: