Global Reference Standards Specialist (Cross-Functional)

Ascendis Pharma A/S is seeking a Reference Standard Specialist to manage activities with CMOs and internal QC teams. You will ensure alignment on reference standards, regulatory input, and inspection readiness, contributing to development and post-approval resupply alongside a global team.

You will work from our Hellerup HQ or collaborate with cross‑functional colleagues across Europe and the United States, driving continuous improvements in reference standard programs and regulatory compliance.