Technology Transfer Lead

Lead the technical transfer and introduction of new sterile drug products from early clinical development through to commercial manufacturing, ensuring a smooth and compliant transition into GMP operations.

Act as the central point of contact for customers and cross-functional stakeholders, coordinating activities, timelines, risks, and milestones throughout the project lifecycle.

Drive process setup, scale-up, and implementation activities for aseptic manufacturing, ensuring successful product launch and operational readiness.

Create and maintain technical documentation, including master batch records, transfer packages, and process implementation documents, while ensuring data integrity and GMP compliance.

Oversee deviation management, CAPAs, and change controls, supporting inspections, audits, and regulatory activities while maintaining the highest quality, safety, and compliance standards.

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees.

This is an office-first role. Working together in person supports close, real-time collaboration and team alignment, enabling us to deliver our best work. You will work primarily in the office, with the flexibility to work remotely for 20% of your time (one day per week).

• Proven experience in aseptic GMP manufacturing, with 3-4 years of relevant experience in the pharmaceutical industry and a strong understanding of sterile operations.

• Solid knowledge of Fill & Finish processes, including hands-on experience supporting manufacturing activities in a regulated environment.

• Strong understanding of GMP requirements and quality standards, with the ability to apply them effectively in day-to-day operations.

• Fluent German and English communication skills, enabling effective collaboration with site teams, global stakeholders, and customers.

• Proactive, detail-oriented, and collaborative mindset, with the ability to coordinate multiple priorities and contribute to the successful introduction of new products into manufacturing.