Job ad: Director CMC Regulatory Affairs

Director CMC Regulatory Affairs

Step into a central role, in which you will lead high-profile CMC submissions that are key for the success of Bavarian Nordic’s ambitious strategy of becoming a best-in-class vaccine manufacturer.

As Director CMC RA, you are going to lead the RA CMC Post Authorization team (4 FTEs) that handles multiple technical transfer (TT) submissions to global markets. It is a position where you will have the chance to leave your mark on ensuring approvals for strategically important manufacturing sites.

It will be your primary task to ensure maintenance of marketing authorization of key vaccines and to lead global CMC regulatory strategy for newly acquired commercial vaccines. In this regard, you will have a focus on maximizing the business benefit in coherence with regulatory risks and compliance.