Regulatory Affairs & Quality Assurance
Newly created position
About Our Client
Our client is a specialised player in the medical device industry. To cope with growing importance of the Hong Kong market, they are currently looking for a high calibre individual to manage Regulatory Affairs and Quality Assurance locally.
Reporting to the Regional Director, you will serve as a technical advisor for local staff, and be responsible for new product registration, product listing, and managing compliance to local regulatory requirements and business requirements. You will be the sole personnel in Hong Kong for managing the Quality Management Systems including but not limited to conducting training and audits, handling complaints, maintaining records, etc.
The Successful Applicant
You will be a Bachelor's Degree holder with at least 3 years of experience in RA / QA from the medical device or pharma industry. You will be familiar with local laws and regulations as well as international standards such as ISO 13485. You will be a self-motivated individual who can work independently.
What's on Offer
Our client provides excellent working culture, benefits and promising career development.