**The Position**

In this role, you will be accountable for defining worldwide regulatory strategies and requirements for biological projects with a strong focus on established vaccines. You will shape the content of regulatory filings for biological products and coordinate agency submissions as well as interactions with external outsourcing partners, where applicable.
As part of the Global Regulatory Affairs organization, you will contribute your veterinary regulatory expertise to cross‑functional project teams and support the strategic direction of RA/PV.
This position is part time eligible with 50%.

**Tasks & responsibilities**

+ In this role, you will define worldwide regulatory strategies and requirements for biological projects with a focus on established vaccines.
+ Within your area of responsibility, you will define regulatory requirements and submission classifications for project activities.
+ By defining robust submission packages, you w...