Overview
In this role you will lead supplier quality activities at Cytiva Newquay, ensuring supplier performance aligns with quality standards. You will collaborate with cross-functional teams to manage audits, CAPA/SCAR processes, and supplier onboarding to support life-saving research and therapies. You’ll drive improvements through root-cause analysis, containment, and proactive supplier development. This position offers a chance to shape supplier quality programs and deliver tangible impact across the organization.
Responsibilities
- Issue, monitor, and approve SCARs and communicate outcomes
- Provide feedback on root-cause analysis with suppliers and support improvements
- Maintain auditor status, train team, and lead remediation after failed audits
- Develop and manage the annual supplier audit program
- Assess impact of changes, communicate with stakeholders and suppliers, and manage change requests
- Containment and correction of supplier defects, own quality event tasks and train colleagues
- Collaborate with cross-functional teams (Engineering, PM, Sourcing, QA) on supplier quality, onboarding, and monitoring
- Create inputs for Management Review and contribute to daily management with action plans
Key requirements
- Bachelor in Engineering or equivalent
- Minimum 5 years of Quality experience in manufacturing/engineering/QA
- Minimum 3 years in supplier onboarding, auditing, and supplier communications
- Knowledge of ISO, CFR, GMP and related regulations
- Collaborative mindset
- Training and mentorship
- Clear communication with suppliers and internal stakeholders
- Supplier auditing
- SCAR/CAPA management
- Change control and supplier onboarding
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