Senior Director - Site Quality

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Your Role: Senior Director – Head of Quality

As the Site Quality Leader, you will own the Quality Assurance and Quality Control functions for the Kiel manufacturing site, leading an organization of approximately 130 personnel. You will provide strategic, regulatory, and technical leadership to ensure the sustainable performance and compliance of this high impact site within the Elanco network.

Your Responsibilities:

• Oversee all aspects of Quality Management to ensure regulatory standards are met, regularly assessed, and reported to global leadership.
• Drive readiness for Health Authority inspections (PAI, directed, etc.) and ensure all GMP follow up actions from audits are effectively actioned.
• Manage the organizational Quality budget and deploy operational excellence strategies to drive lab and site-wide productivity.
• Recruit and develop global talent to build a high-performance culture and a robust succession pipeline for critical Quality roles.
• Partner cross-functionally with Manufacturing, Supply Chain, and R&D to ensure quality objectives are achieved during product transfers and new launches.

What You Need to Succeed (minimum qualifications):

• Education: Bachelor’s Degree in a scientific field.
• Experience: A minimum of 10 years of management or project management experience in the pharmaceutical industry (DP/API), including at least 5 years specifically in Quality Assurance.
• Comprehensive knowledge of global cGMP requirements and a proven track record in inspection management with authorities such as the FDA and EMA; fluency in English.

What will give you a competitive edge (preferred qualifications):

• Technical understanding of DP/API manufacturing and testing processes.
• Demonstrated ability to lead through transformation and drive digital roadmaps.
• Strong competency in Quality Risk Management techniques and problem-solving in ambiguous environments.
• Experience in both site-level and network-level Quality leadership.

Additional Information:

Location: Kiel Manufacturing Site, Kiel, Germany -

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