GLP/GCLP Vendor Oversight and QA Lead (EU)

GLP Vendor Oversight and QA Lead

The integrity of nonclinical data depends on more than what happens inside a company’s walls. Much of the critical work in GLP‑regulated research—safety studies, toxicology, analytical testing—is carried out by external laboratories and CROs. When that network of partners operates to the highest quality standards, the science is sound. When it doesn’t, the consequences reach all the way to patients.

Why this role matters

GLP vendor oversight is often invisible when it’s done well – and very visible when it isn’t. As the internal authority on GLP and nonclinical vendor quality, you will be the person others turn to when the questions are difficult. If you take data integrity seriously, understand the regulatory landscape deeply, and want to shape how a global company manages its external nonclinical network, this is a role with real scope to make a difference.

About The Role

Own quality oversight of ext...