Regulatory Affairs Project Manager
KI-Beschreibung
As an International Regulatory Project Manager, you will play a key role in ensuring high-quality regulatory submissions for IVDs. Your day-to-day responsibilities will involve coordinating documents, maintaining approvals, and collaborating with various stakeholders to navigate the regulatory landscape.
Anforderungen
5–7 Jahre- •At least 5 years of experience in Regulatory, R&D, Quality, Operations, and
/ or Clinical - •Bachelor’s or Master’s degree in Life Science, Data Science, or related subject, or equivalent experience
- •Experience in diagnostics or pharmaceutical regulatory affairs