Pharmacovigilance QA Auditor Specialist

Role: Pharmacovigilance QA Auditor Specialist to ensure quality and compliance across Johnson & Johnson's pharmacovigilance activities. Responsibilities include leading routine PV internal and external audits, supporting audits of data, facilities, and processes in GxP/non-regulated areas, and assisting with regulatory inspections. The role involves collaboration with business partners, providing compliance guidance, and potentially developing training materials. Requirements: minimum 4 years in Pharmacovigilance, strong project management, data analysis, and communication skills; proficient with Microsoft Office. Preferred: broad auditing experience, familiarity with various audit types, and understanding of auditing landscapes. HighValue: pharmacovigilance, PV audits, GxP compliance, regulatory inspections, 25% travel. Location: Raritan, NJ; Titusville, NJ; Horsham, PA; hybrid work setup.