RA/ QA Director
Strategic partner of group CEO in optimizing operation
Global head of RA/ QA department
About Our Client
A global Medical Device provider actively involved in developing, manufacturing and marketing intensive care products.
- Reports to Group CEO
- Oversee the strategic direction, preparation and progress of regulatory agency and notified body submissions
- Organize and lead the knowledge construction of existing and emerging regulations, standards, or guidance documents.
- Serve as a management representative for regulatory agency, notified body and customer audits.
The Successful Applicant
- Extensive knowledge in TFDA, FDA and CE regulations
- RA experience in Medical Device is a must
- Logical and willing to take on challenge to transform the business
- Fluent in English and Mandarin
What's on Offer
Global scope, competitive bonus