Proven leadership experience: Minimum 4 years managing and developing high-performing teams in a technical quality environment, with a focus on coaching, mentoring, and setting strategic goals., Strategic mindset: Demonstrated ability to define and execute global supplier quality strategies, roadmaps, and programmes that align with organisational objectives., Extensive industry expertise: 10+ years in supplier quality within medical devices or in-vitro diagnostics (IVD), including experience influencing global processes and driving continuous improvement., Regulatory and compliance knowledge: Deep understanding of GMP, ISO 9000, ISO 13485, and 21 CFR 820, with a track record of supporting FDA and Notified Body audits., Performance-driven approach: Skilled in monitoring and interpreting KPIs such as PPM (Parts Per Million), on-time delivery, and quality metrics to inform strategic decisions., Global collaboration: Ability to work effectively across regions and functions, fostering partnerships that enhance supplier capability and organisational resilience., Flexibility for travel: Willingness to travel up to 20% (primarily within Europe, occasional global trips) to strengthen supplier relationships and oversee compliance initiatives., Root Cause Analysis & Corrective Actions: Strong problem-solving skills using tools like 8D, FMEA, SPC, and Six Sigma., Presentations and metric reporting to executive leadership

sharing the costs of sports activities, private medical care, sharing the costs of professional training & courses, life insurance, flexible working time, integration events, coffee / tea, drinks, parking space for employees, leisure zone, extra social benefits, holiday funds, employee referral program, charity initiatives, family picnics