Director Quality Assurance Operations, Boxmeer

About the role

We are seeking a Director of Quality Assurance Operations for our Animal Health facility in Boxmeer. This role reports to the Site Quality Lead and forms part of the Site Quality Management Team. You will translate global, regional and site quality priorities into an operational strategy that ensures compliant, uninterrupted supply of vaccines and pharmaceuticals while driving continuous improvement and digitization across site quality processes.Tasks and Responsibilities

Lead and develop the QA Operations team (5 direct reports, ~100 employees). Translate Quality organization strategy into QA Operations plans. Design, plan and implement the operational QA strategy in line with global, regional and site quality goals. Manage QA Operations budget and required reporting.Shape, implement and continuously improve strategic plans for QA Operations. Oversee batch release processes and end‑to‑end batch tracking. Monitor KPIs, use metrics for decision‑making and take corrective actions when needed. Identify business trends through metrics and adjust actions accordingly.Initiate, prioritize, manage and coordinate improvement initiatives for QA Operations in collaboration with other site functions. Develop, implement and maintain standards, procedures and guidelines within the Manufacturing Division, especially in review and release areas. Ensure QA Operations processes comply with relevant regulations and requirements.Solve problems, escalates issues appropriately to global teams and keep relevant stakeholders informed. Determine the QA Operations project portfolio in alignment with partner IPTs. Lead and/or participate in site projects and provide quality oversight and support. Develop a strategy for smooth batch flow, including multi‑site product releases.Build robust inter‑site processes, clear communication flows and defined handoffs between sites and functions. Work closely with global quality management, health authorities and site operations management. Qualifications

Academic degree in a relevant field (Pharmacy, Medical Biology, (Bio)Chemistry, (Bio)Process Technology or related scientific fields). 7–10 years of relevant experience in an international pharmaceutical company. Proven track record of managing and developing large organizations and leading other managers in a complex and relevant organization.Strong leadership capabilities, with the ability to inspire, develop and align diverse teams across regions and functions. Demonstrated success in stakeholder management, building trusted partnerships and influencing effectively across organizational levels. Solid understanding of GMP, quality systems and relevant manufacturing regulations.Experience working with health authorities and managing audits and inspections. Excellent command of the English language, oral and written. What We Offer

Competitive compensation aligned with knowledge and experience. 3% year‑end payment and an annual bonus based on individual and company performance. Company car or car allowance. A minimum of 25 days of leave. Solid Pension Plan. Excellent accessibility: train station adjacent to main entrance and ample parking.High‑quality company restaurant with fresh, healthy options daily. Contribution toward personal sports/fitness membership to support vitality. Beautiful private park on the premises, ideal for walk, break or relaxation. Mental well‑being support via Lyra Health for you and your family members.Access to a dedicated prayer/meditation room. About the Company

Merck&Co., Inc. (Merck Sharp&Dohme LLC) is a global health‑care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The company is committed to preserving and improving the health, well‑being and performance of animals and the people who care for them through veterinary medicine and digital solutions.

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