about the company
A medical devices company with presence globally
about the job
you will be preparing and submitting regulatory applications to authorities in the APAC region. You will be required to maintain and renew regulatory licenses in the APAC region in a timely manner. Besides, to develop regulatory strategies and project timelines for new product registrations or change submissions based on input from key cross-functions.
you will also be responsible in QA activities which includes post market vigilance, complaints investigation and maintaining the QMS.
about the manager/team
This role will be an individual contributor and reports into RAQA Manager, APAC
skills and experience required
You must be equipped with at least a Degree in Lifesciences, Engineering or equivalent and have at least 3 years of RA experiences in the medical industry.
**Candidates with more experience will be considered for a Senior Executive position.
To apply online, please click on the appropriate link.
EA: 94C3609 / R1215243