About this role
Lead strategic regulatory programs and provide expert consulting for MedTech clients across Japan and the Asia-Pacific region. Develop regulatory strategies for product registrations, market access, and compliance for medical devices and digital health technologies.
Requires a bachelor's degree in life sciences or engineering and over 12 years of regulatory affairs experience in the healthcare industry. Must have significant experience with Japan and Asia-Pacific regulatory frameworks and a proven track record of leading complex global submissions.
What they're looking for
Regulatory StrategyMarket AccessMedical Device RegulationsStakeholder ManagementProject ManagementComplianceClinical EvidenceRisk Management
Frequently asked questions
What does a Director of Regulatory Affairs, JAPAC MedTech at IQVIA do?
Lead strategic regulatory programs and provide expert consulting for MedTech clients across Japan and the Asia-Pacific region. Develop regulatory strategies for product registrations, market access, and compliance for medical devices and digital health technologies. Requires a bachelor's degree in l…
What skills does this Director of Regulatory Affairs, JAPAC MedTech role need?
Key skills for this role include Regulatory Strategy, Market Access, Medical Device Regulations, Stakeholder Management, Project Management, Compliance.
How much does a Director of Regulatory Affairs, JAPAC MedTech at IQVIA pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Director of Regulatory Affairs, JAPAC MedTech role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Director of Regulatory Affairs, JAPAC MedTech role?
You can apply directly on IQVIA's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.