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.
Shape Agile Pharma Drive Compliance Innovation and Continuous ImprovementAre 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 bus...
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.
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