Process Expert, Drug Product

Act as the technical expert to ensure that the production line runs efficiently and effectively. Coordinate and support the qualification of the manufacturing line, ensuring they meet strict industry standards. Identify weaknesses in the production line and determine solutions to fix or investigate issues. Establish, drive and maintain good cleanroom management practices. Collaborate with team members and various internal functions (e.g. MSAT, QA, Engineering) to successfully implement improvements and new processes.

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. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

• Degree or equivalent experience in Life Science or Engineering

• Proven experience in EITHER aseptic filling or aseptic manufacturing in the GMP controlled environment is a must, additional experience in the qualification of manufacturing equipment is highly preferred

• Experience with lyophilization processes is highly preferred

• Proficiency in English is a must; German is a plus

• Ability to agilely move between various tasks during this dynamic and exciting project phase. You demonstrate strong collaboration skills and actively support your team members