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- Responsible for Singapore and the assigned countries within SEA.
- Work with Global Regulatory Affairs to plan, schedule, and manage the process of preparing, coordinating and submitting regulatory applications to local Regulatory Authority.
- Support local EU MDR regulatory submission and approval.
- Ensure regulatory approvals are obtained for all marketed devices and general management of registration functions are performed in accordance with regulatory guidelines and company internal procedure.
- Proactively monitor, review and manage internal tracking for licenses that are expiring.
- Update and maintain regulatory submissions and approvals in the designated systems / database in accordance to the internal requirements.
- Work with local Supply Chain and Commercial teams to mitigate supply risks.
- At least a Diploma/Degree
- Fresh graduate with minimum or no working experience
- Training will be provided
- Proficient in the use of MS Word, Excel and PowerPoint
- Good spoken and written of English language
- Able to work independently and possess great sense of responsibility and accountability
RA Project Specialist - Singapore - Abbott Laboratories
Description
RESPONSIBILITIES
QUALIFICATIONS