Description
BioMarin is hiring an Associate Director, GVP Compliance in London, United Kingdom, to advise stakeholders on Good Pharmacovigilance Practices, assess compliance with global regulations and corporate policies, conduct GVP audits, support regulatory inspections and mock readiness, and help resolve compliance risks. The role requires at least eight years of experience in a regulated healthcare industry, including quality and compliance, pharmacovigilance, health authority inspections, R&D audits, and GVP audit programs. It is a hybrid position with two days per week onsite, may be performed remotely for EU and US time zones, and may require travel of 25% or more.
