.Detalles del empleoTipo de empleo: Jornada completaUbicación: Madrid, Madrid provinciaDescripción completa del empleoOur Quality Assurance group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network dedicated to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.We are seeking a growth and improvement minded External Quality Associate Director that can help drive our Strategic Operating Priorities in Europe and APAC regions.Invent: Pursue the Most Promising Internal and External Science to Address Significant Unmet Medical NeedsExecute: Prioritize Resources Behind Our Key Growth Drivers (Oncology, Vaccines, Select Specialty Areas, Animal Health) While Optimizing Our Base BusinessAdapt: Develop Our People, Culture and Business Model to Evolve with a Dynamic LandscapeDiverse Talent: We are committed to providing an inclusive and welcoming environment with supporting leadership behaviors because having a high-performing, engaged workforce is critical to our ability to deliver innovative solutions to patients and customers around the worldValues and Standards: Our Steadfast Commitment to Our Values and Standards will Continue to Guide Us as We Take on New Opportunities and Will Always be Fundamental to Our Success – They are a Competitive Advantage for UsKey ResponsibilitiesProvides Quality oversight over one or more External Entities or projects that will manufacture or test cell banks, biologic drug intermediates, biologic drug substances, or biologic drug products or both on behalf of our Company for product and analytical technology transfer.Serve as the quality project lead for Technology Transfer, New Product Introduction and Analytical Transfers to Contract Manufacturing and testing sites.Assist in managing the end-to-end processes of transfers including but not limited to: Due Diligence, Feasibility Studies, Protocols/Reports, PPQ, PAI Readiness and Quality System Oversight Implementation.Works with a team of quality project leads and cross functional transfer teams.Reports to the Quality Director, EQA, for general advice and instruction concerning Quality Operations, but functions independently.EducationBachelor's or Master's degree in a Science, Engineering, or related area of study
