- Manage and execute regulatory projects for product registrations in APAC countries, including dossier preparation and submission, authority liaison, and approval negotiation.
- Ensure timely renewal of existing product licenses in accordance with local regulations and guidelines.
- Monitor and communicate regulatory changes and updates in APAC countries and share the information within the organization.
- Interpret and provide regulatory guidance to cross-functional team including manufacturers, scientists, and marketing and sales colleagues
- Address customers’ inquiries and resolve issues related to regulations and compliance matters.
- Manage the Product Label System and Dossier Database Sharepoint.
- Support the Regulatory Affairs functional Head in various other activities as assigned
Requirements
- Min Diploma / Degree in any courses
- Min 2 to 3 years of regulatory experience (Medical Device / Pharma)
Interested candidates, please forward your resume to [email protected]
Consultant: Huang Jingsheng Kevyn (R1333338)
Recruit Express Pte Ltd (99C4599)
Recruiter Ref code: #HKH
