Are you interested in working for a global company where you can work across functions and on a wide-variety of projects? As a member of Stryker's RA/QA team, that is exactly what you will do! Here, we provide our RA/QA team the opportunity to learn new things, as well as endless growth opportunities! If you are interested in working at one of the World's Best Workplaces, apply now !

Need another reason to apply? Here are 10 reasons to join our Regulatory Affairs/Quality Assurance team: https://www.strykercareersblog.com/post/10-reasons-to-join-strykers-regulatory-affairs-team

About the job:

The role is responsible for maintaining Hong Kong's Tender database, global Regulatory Affairs (RA) database, Hong Kong medical devices registration and Quality Assurance (QA) work.

• Maintain Hong Kong's RA database, including global registration database and local Tender database.
• Provide RA supports to local Quotation/Tender.
• Submit license renewal/change or other local registration to achieve the company goal.
• Represent as a local RAQA contact to assist on local communication with all stakeholders, manage product complaints, commercial hold and field actions in HK.
• Other tasks as assigned by manager.

• University or master's degree holder in healthcare/medical/engineering related major is preferred but not limited to.
• Relevant regulatory and quality assurance experiences for minimum 1 - 2 years.
• Good with Microsoft Word, Excel etc.
• Team player and have the ability to interact, influence and partner with leaders.
• Detailed oriented.
• Excellent communication skills with proficiency in spoken and written English and Chinese.
• Ability to move others to take action.
• Hands-on ability to implement swiftly and effectively by taking ownership and accepting responsibility.
• High ethical standards and integrity.
• Well-organized and logical thinking.
• Patient and a great sense of responsibility and accountability
• Interested to explore more in RAQA field.