Global GxP Quality System Manager – Contractor
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 GxP 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).
* Start Date: May 2026
* End Date: December 2026
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.
Interested? We are looking forward to get in touch with you. Online application
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