Regulatory Affairs Manager (Companion Diagnostics, CDx)

at  Roche

Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.
The Position
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.
At Roche Global Regulatory Affairs we strive to be the world’s best Regulatory organization, championing patient access to the world’s best diagnostics. The focus of our work in this team is the global approval of in-vitro-diagnostics of the Molecular and Pathology Companion Diagnostics product portfolio. Our team is tasked with regulatory projects as well as overarching regulatory topics. You can expect an open-minded work environment, where you will be working closely with colleagues in other departments and other counties.

Please refer the Job description for details