Pharmacovigilance QA Auditor Specialist

Role: Pharmacovigilance QA Auditor Specialist responsible for leading PV internal and external audits, supporting regulatory inspections, and ensuring compliance across GxP and non-regulated areas within Johnson & Johnson's Innovative Medicine division. Responsibilities: plan, conduct, and report audits; collaborate with business partners on compliance inquiries; support audit preparations and may assist in training material development. Requirements: Bachelor’s degree (preferably in life, natural, or computer science); at least 4 years of relevant PV experience; strong project management, data analysis, and communication skills; proficiency with Microsoft Office. Preferred: understanding of auditing processes and experience with various audit types. High-Value: focus on pharmacovigilance, GxP compliance, internal/external audit leadership, regulatory inspections, and global collaboration. Work setup involves 25% domestic/international travel. The position is based in Horsham, PA; Raritan, NJ; or Titusville, NJ.