Good Clinical Practice QA Manager (m/f/d)
On-site · Allschwil, Basel-Landschaft, Switzerland
Job Summary
Lead and ensure compliance of global CQA processes across multiple sites. Act as key Quality partner for cross-functional stakeholders (Clinical Trial Teams, Biometry, CROs). Drive continuous improvement initiatives and proactively identify risks and opportunities. Collaborate closely with international sites to align quality standards and best practices. Lead and support audits, health authority inspections, and regulatory interactions. Provide expert guidance on complex quality topics and decision making. Foster strong stakeholder relationships through clear and effective communication. Take ownership of critical quality topics and drive them to resolution with accountability.
Required Qualifications
- Degree in life science or health care
- Proven senior-level experience in CQA / Quality within a regulated environment (Good Clinical Practice)
- Demonstrated experience working in a global and cross-functional setup
- Strong communication and stakeholder management skills across all levels
- Proactive, hands-on mindset with the ability to take initiative and drive topics forward
- Structured, solution-oriented approach with a clear sense of ownership
- Passion for collaboration and working closely with people across functions and cultures
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