Shape Agile Pharma – Drive Compliance, Innovation, and Continuous Improvement Are you an experienced QMS specialist seeking a high-impact consulting assignment in the pharmaceutical industry? Join us as a Global Gx P Quality System Manager and help transform our agile Quality Management System to meet business priorities and regulatory demands. You will work at the forefront of rare-disease biopharma, ensuring efficient QMS governance, proactive risk management, and excellence in global process alignment. Your responsibilities: Lead QMS Development & Governance: Drive ongoing QMS improvements, harmonize processes, and streamline change management for optimal compliance. Manage Risk & Compliance: Identify and mitigate QMS risks, collaborate with cross-functional stakeholders to maintain a robust global quality culture. Champion Continuous Improvement: Monitor KPI trends, support Quality Management Reviews, and lead strategic initiatives to boost QMS performance. Global Collaboration: Interface with Global Process Owners to ensure consistent training standards, regulatory surveillance, and readiness for inspections. Your profile:5+ years of experience in the pharmaceutical industry (Quality Systems, Manufacturing, or R&D). Proven expertise in QMS implementation, procedural document writing, KPI management, and global quality oversight. Fluent in English, with strong communication and leadership skills. Proactive mindset, adept at driving cross-functional alignment and handling complex scenarios. Project Details: Location: Basel, Switzerland (on-site/consultant arrangement). S__tart Date:__ May 2025 End Date: November 2025 Ready to Shape the Future of Our Global QMS?Take on this dynamic consultancy role and make an immediate impact in rare-disease biopharma. Apply now to lead our QMS transformation and help ensure patients worldwide receive life-changing therapies.
#J-18808-Ljbffr