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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!
Lohmann Animal Health GmbH – a global leader specializing in the production of poultry vaccines – has been part of Elanco since 2014. With our innovative products and services, we strive to take responsibility for the community and enrich the lives of both people and animals. Our vaccines are exported to more than 70 countries worldwide. With more than 180 employees and a long-standing company history, Lohmann Animal Health GmbH offers an exciting, international, and impactful working environment.
We are seeking an experienced Sr. Director, Pharmaceutical Technical Services/Manufacturing Science (m/f/d) to join our Technical Services/Manufacturing Science team in our manufacturing site in Cuxhaven.
Technical Stewardship & Process Optimization: Lead ongoing monitoring, improvement, and validation of commercial manufacturing processes, championing sound scientific principles, driving the site's technical agenda, and providing high-level guidance for complex technical investigations.
New Product Introduction & Tech Transfer: Lead seamless technical transfers of new products and processes from R&D or other sites to Cuxhaven, building strong cross-functional partnerships, and ensuring technical readiness for new product launches.
Quality, Regulatory & Compliance: Serve as a primary participant and SME during regulatory agency audits, actively leading site-wide quality improvement initiatives, and overseeing the technical accuracy of regulatory submissions.
Organizational & People Development: Direct and mentor a high-performing team of scientists and engineers, fostering a culture of continuous process optimization and innovation, and setting clear performance objectives aligned with site and global strategies.
Minimum of 15 years of relevant pharma/biopharma experience, including 10 years in leading teams or organizations.
Minimum 5 years of expertise in the field of commercial manufacturing of vaccines.
Experience with an EU GMP controlled environment.
What will give you a competitive edge (preferred qualifications):
Advanced Degree (Master, PhD)
Knowledge of vaccine-based technology platforms (fermentation, egg-based) and relevant experience in associated disciplines such as Manufacturing, Development, Engineering, Quality Control, Quality Assurance, Advanced Project Management, Regulatory, or Administration.
Strong scientific and analytical thinking, with the ability to manage complex situations and conflicting priorities.
Proven ability to influence people, build collaborative relationships across functions and with external partners, and communicate effectively.
Employer contribution to pension plans
40-hour work week
30 days of annual leave
Meal allowance subsidy
Regular team events
Health and fitness programs as well as access to Corporate Benefits
Freedom for personal initiative and opportunities for individual professional development
Working in a dynamic team within an international company

27472 Cuxhaven,
Niedersachsen DE