Quality Systems & Compliance Specialist

Jubilant Radiopharma in Caen, France, seeks a detail-oriented Specialist, Compliance to support Quality Management System maintenance and regulatory compliance across the organization. You will collaborate with cross-functional teams on audits, CAPA, change control, investigations, and continuous improvement initiatives.

The role requires in-depth knowledge of GxP regulations (US, Canada, Europe), FDA 21 CFR 820, ISO 13485, EU MDR, and fluent FR/EN communication with regulators and partners.