Key responsibilities:

• Ensure that operational activities for clinical and/or commercial manufacturing are performed in a timely manner and within given safety and quality standards.

• Responsible for entire processes or process units for clinical and commercial manufacturing projects in therapeutic BioConjugates like Antibody-Drug Conjugates (ADC).

• Complete commissioning, qualification, and validation activities for bioprocess equipment and systems.

Key requirements:

• Master's Degree in Biotechnology, Biochemical Engineering, Biochemistry, or a related Life Science subject. Equivalent experience will also be considered for candidates with a Bachelor's Degree.

• First GMP experience and understanding of bioprocess technology

• Demonstrated ability to efficiently implement CQV strategies in complex bioprocessing systems.

• Knowledge of Antibody-Drug Conjugates (ADC) and their bioprocessing requirements.

On top of being an equal opportunity employer and value diversity at our company, we offer great benefits and a comprehensive relocation package for eligible talents!

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.