Associate Specialist, Regulatory Affairs
Hybrid
Core
Support product life cycle management and regulatory submissions for new products, changes, and renewals in the EMEACLA region.
Role type
Associate Specialist, Regulatory Affairs
Builds
Regulatory submissions and playbooks for medical devices
Domain
Medical devices / Regulatory Affairs
Deliverable
client delivery
Required skills
Regulatory strategy development, process improvement, documentation management, stakeholder guidance, bid/tender support, timeline tracking
Preferred skills
Data management, analytical skills, system proficiency, attention to detail, cross-functional collaboration
Technologies
Regulatory submission systems, dashboards, reports