CH12 Lonza AG
Associate Director, Global Good Manufacturing Practices (GMP Compliance) (Biotech)
Today Lonza is a global leader in life sciences. We are more than 15,000 employees in more than 100 locations around the world. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
To strengthen our Lonza Global Good Manufacturing Practice (GMP) Compliance Department, we are looking for an exceptional Associate Director, Global GMP Compliance reporting to the Head Global GMP Compliance. The purpose of the role is to plan and execute a program of corporate GMP compliance audits/assessments for Lonza's GMP sites and operations with a focus on sterile and non-sterile drug products (including cell and gene therapy, biologics, oral dosage forms), biological and chemical Active Pharmaceutical Ingredients, medical devices but also covering food, feed and dietary supplements. The role will involve a large amount of international travel (up to 50%).
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.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.