Jobs at MSD Animal Health Technology Labs

Lead and perform GMP/GDP audits across global manufacturing sites, suppliers and distribution partners; assess compliance, support supplier qualification and inspection readiness, report findings, drive risk mitigation and continuous improvement, and collaborate with cross-functional stakeholders while traveling regularly across Europe and internationally.

Lead and develop regional regulatory strategy for a complex oncology portfolio across Europe, UK, Switzerland and select non-EU markets. Manage regulatory submissions (PIPs, ODD, Scientific Advice, EU registrations), advise global and local stakeholders, liaise with health authorities, ensure compliance and lifecycle management, and lead people, projects and process improvements to secure timely approvals and optimal labeling.