Roles & Responsibilities
📍 Location : Suntec
🕒 5 Days | Office Hours
Key Responsibilities
- Coordinate product registration (new and renewal) in designated countries, including preparing dossiers and certificates within specified timelines.
- Act as the main liaison between factories and regulatory teams across assigned markets.
- Provide regulatory assessment for new product introductions and product changes.
- Advise internal and external stakeholders on interpreting relevant regulatory guidance and standards.
- Support preparation of regulatory documents for tender submissions.
- Perform other ad-hoc duties as assigned.
Qualifications
Min. Bachelor’s Degree in a relevant discipline.Min 3 years of relevant experience in regulatory affairs and / or quality assurance within the medical devices sector.Strong knowledge of regulatory requirements and standards for medical devices.Good communication, coordination, and problem-solving skills.If interested, please email me at alexgoh@recruitexpress.com.sg or telegram @alexgohhl
Alex Goh Hock Leong
(CEI.No : R1763413 l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)
Tell employers what skills you have
Quality Assurance
Regulatory Affairs
Healthcare
Interpreting
Compliance
Tender Submissions
Medical Devices
Audits
Regulatory Requirements
Regulatory Submissions
Manufacturing