Offer summary
Qualifications:
Degree in Natural or Engineering Sciences, Minimum five years experience in medical device regulation, Knowledge of international standards for China, Fluency in German, English and Mandarin, Good understanding of technical documentation.Key responsabilities:
- Coordinate international registration projects closely with teams
- Manage project implementation and process improvements
- Prepare and adapt regulatory applications to local laws
- Participate in project groups for medical device approvals
- Maintain and update electronic databases
