Overview As a Global GCP/PV Auditor, you will ensure clinical and pharmacovigilance activities meet regulations and Novartis standards. You will plan, lead and report independent audits, support CAPA activities, and drive continuous quality improvements across global operations. The role involves stakeholder guidance, training, and collaboration with cross-functional teams to uphold GCP/GPvP compliance.

This position offers remote work within Spain with travel up to 50% and relocation support. Compensaciones / Beneficios versátil and hybrid working options global recognition programs Responsabilidades Plan, lead, conduct, document, and follow up on GCP/PV audits in line with Novartis procedures and regulations Perform low-risk audits (investigator site, single-service vendors,



systems/process, patient-oriented programs) Support complex audits (country organizations, multiservice vendors, high-risk vendors) Provide technical guidance and training to ensure consistent audit execution and quality Escalate critical findings and coordinate immediate follow-up actions 1–2 years of GCP auditing experience preferred Strong quality, compliance mindset and stakeholder engagement skills Fluent English; additional languages advantageous Audit management and CAPA processes Quality assurance training and guidance

📌 Global Good Clinical Practices / Pharmacovigilance Auditor (Barcelona)
🏢 Novartis
📍 Barcelona