Role has been created to support the growing business in BioConjugates.

Key responsibilities:

• As a member of the quality assurance team (PCP Conjugates), you will be responsible for the ensuring production of APIs is in accordance with Good Manufacturing Practice (GMP)

• You will support the contract manufacturing and advise members of development, production and analytical departments on all aspects of GMP

• You will be responsible for checking manufacturing documentation for conformity, change control and investigation of deviations and OOS-results

• In addition, you will be the quality contact for our clients, and will be present during their GMP audits

Key requirements:

• A degree in Life Science (microbiology, biotechnology, chemistry)

• Relevant experience in the biopharmaceutical industry, ideally in GMP area, is preferred

• Excellent English (writing and speaking) is required to interact with our international clients

• Good basis in German to interact with colleagues on a daily basis

• We are looking for someone who is independent, sociable, customer focused and who values working as a team player

• In addition, good communication skills and ability to combine regulatory awareness with an entrepreneurial mindset, would be optimal 

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.