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Manages a portfolio of capital investment, renovation, and construction projects at Merck's Animal Health site in Boxmeer, coordinating project leaders and engineering teams while ensuring GMP compliance and EHS standards.
The Senior CSV QA Specialist leads risk-based computerized system validation and ensures data integrity and GMP compliance across manufacturing and laboratory systems. The role involves providing quality oversight, managing inspection readiness, and driving standardization within the global Digital & Data Quality team.
Job Description Director Operations for Drug Product Do you aspire to secure a critical role in the production of biologics-based medicines? Are you excited to lead dynamic teams in a state-of-the-art facility that…
Leads regulatory submissions and compliance for assigned drug products in Canada, interfacing with Health Canada and global teams to ensure adherence to local and international standards.
Job Description We aspire to be the premier research-intensive biopharmaceutical company. At the forefront of research, we deliver innovative health solutions that advance the prevention and treatment of diseases in…
Job Description Clinical Trial Coordinator Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving…
Job Description The Executive Director (Distinguished Scientist) and Product Development Team (PDT) lead has primary responsibility for the planning and directing of clinical research activities involving new or…
Job Description ¿Eres estudiante y buscas una experiencia que impulse tu desarrollo profesional? Esta es una excelente oportunidad para adquirir experiencia práctica en una compañía líder, participando activamente en…
Oversee engineering and technical projects in a biopharma production site, coordinating suppliers, budgets, and GMP compliance while driving cost and energy savings.
Job Description An outstanding opportunity for a highly skilled technical leader to join the downstream technical operations function at our state-of-the-art biologics manufacturing site in Dunboyne, Co. Meath. The…
Job Description Do you want to work at one of the largest industrial pharmaceutical companies in the Netherlands within a high-tech environment and apply your knowledge and skills? Have you always wanted to work in a…
Job Description Wil jij werken bij een van de grootste industriële farmaconcerns van Nederland binnen een hightech omgeving en jouw kennis en kunde inzetten? Heb je altijd al willen werken in een bedrijf waar je werk…
Job Description The Associate Director leads and develops a programming and reporting team - set goals, assign work, coach performance, and manage recruiting/onboarding - while communicating status and risks to…
Scrum Master to lead agile teams building Merck’s data infrastructure, coordinating sprints and removing blockers for data context layer development.
Job Description The Opportunity Based in Hyderabad, join a global healthcare biopharma company and be part of a 130- year legacy of success backed by ethical integrity, forward momentum, and an inspiring mission to…
Job Description Join a global qualityorganisationand play a key role in safeguarding product quality, compliance, and patient supply across an international manufacturing and supply network. As an Associate Director…
Job Description An amazing opportunity has arisen for a Quality & Regulatory Specialist in our company Animal Health Portugal. This position will be responsible for supporting Quality and Regulatory activities…
Job Description This is a highly visible leadership role at the forefront of Oncology Regulatory Affairs, offering the opportunity to shape regional regulatory strategy, develop talent, and drive impact for patients…
Job Description Clinical Operations Manager - Regulatory This role is accountable for performance and compliance for assigned protocols in Canada, in accordance with Good Clinical Practices as described by the…
Job Description Join our state-of-the-art biologics manufacturing facility in Dunboyne as the Upstream Technical Operations Lead. In this pivotal role, you will hold end-to-end technical, manufacturing, and people…
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