Ass. Director GPS Quality Management

📋 Description

• Lead global pharmacovigilance audit readiness and inspections
• Oversee GPS issue management, deviations, CAPA and root cause analysis
• Develop pharmacovigilance training programs and curricula
• Manage procedural documentation and continuous improvement
• Coordinate quality performance, KPI development and SOP compliance
• Support PV agreements and cross-functional collaboration

🎯 Requirements

• Bachelor’s degree in pharmacy, nursing, healthcare, life sciences, or related field
• 10+ years in pharma/biotech with 5+ in pharmacovigilance or drug safety
• Experience building pharmacovigilance quality systems and teams
• Strong track record hosting global regulatory audits
• Deep knowledge of PV regulations in Europe, US, Japan
• GxP quality, training program development, and quality records management

🎁 Benefits

• Competitive base salary with location-sensitive range
• Eligibility for incentive programs
• Rewards supporting health, security, well-being, work-life balance
• Remote opportunities for eligible U.S. ETZ and select international locations
• Cross-functional exposure in a growing biopharma
• Meaningful work supporting patients with autoimmune diseases