At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.About the Katwijk SiteEli Lilly is investing €2.6 billion in a new state‑of‑the‑art manufacturing facility in Katwijk, Netherlands. This facility will produce oral medicines for cardiometabolic health, neuroscience, oncology, and immunology, incorporating next‑generation manufacturing technologies including dock‑to‑dock automation, paperless manufacturing, and process analytical technology while achieving carbon neutrality and zero waste to landfills.Position OverviewThe Senior Director – Quality Assurance, Manufacturing is accountable for setting and executing the site Quality Assurance strategy, ensuring sustained cGMP compliance, regulatory readiness, and a strong quality culture across manufacturing operations. This role serves as a senior member of the site leadership team, providing decisive quality leadership, independent oversight, and enterprise‑level influence to protect patient safety and product integrity.Key ResponsibilitiesExecutive Quality LeadershipDefine and own the site Quality Assurance strategy aligned with Lilly Global Quality Standards and business objectives.Serve as the senior quality authority for manufacturing operations, with final decision‑making accountability on quality matters.Act as a visible role model for quality culture, integrity, and patient focus across the site.Governance, Compliance & Regulatory ReadinessEnsure sustained compliance with cGMPs, regulatory requirements, and internal quality systems.Maintain continuous inspection readiness and act as the primary Quality Assurance representative during regulatory inspections.Establish and oversee robust governance for deviations, change management, validation, data integrity, and CAPA effectiveness.Engage constructively with the site Works Council (ondernemingsraad) on quality-related matters affecting working conditions.Manufacturing & Operational OversightProvide strategic quality oversight for manufacturing processes, facilities, utilities, equipment, and computerized systems.Ensure quality risks are proactively identified, assessed, and mitigated.Drive integration of quality into operational excellence, digital manufacturing, and continuous improvement initiatives.Leadership, Talent & Organization DevelopmentBuild, lead, and develop a high‑performing Quality Assurance organization with clear accountability and succession planning.Ensure quality independence while enabling effective cross‑functional collaboration.Attract, develop, and retain senior quality talent to support long‑term site and enterprise needs.Strategic Planning & Business PartnershipServe as a core member of the Site Leadership Team, contributing to site strategy, investment decisions, and long‑term operating model.Influence enterprise quality strategy through collaboration with global and affiliate stakeholders.Ensure quality considerations are embedded in capital projects, technology implementation, and site expansion activities.Environmental Health & SafetyDemonstrate executive accountability for environmental, health, and safety standards within the Quality organization.Ensure safe, compliant operations and strong EHS performance across manufacturing quality activities.Qualifications and RequirementsEducationMaster's degree or PhD in Pharmacy, Chemistry, Engineering, or a related life sciences discipline preferred; Bachelor's degree minimum.ExperienceExtensive leadership experience within pharmaceutical manufacturing or other highly regulated industries.Proven senior‑level accountability for Quality Assurance, regulatory compliance, and inspection management.Experience with EMA, FDA, or other major regulatory inspections (given the new facility context). Familiarity with Dutch regulatory environment and EMA expectations is preferred.Experience in a greenfield or site start-up environment.Experience with oral solid dosage and/or Active Pharmaceutical Ingredient (API) manufacturing.Technical & Leadership ExpertiseDeep expertise in cGMPs, quality systems, and regulatory expectations.Strong strategic leadership, decision‑making, and executive communication skills.Ability to influence at site, regional, and enterprise levelsFluency in English required; Dutch language proficiency strongly preferred.Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly