The Cleaning Validation Expert will own cleaning validation activities for the assigned biological assets at the Visp site. The role includes preparation of validation documents and support of execution, presentation of cleaning validation topics in audits and inspections, tight collaboration with operations and quality to ensure successful and on time validation activities.

Key Responsibilities:

• Develop and prepare equipment cleaning validation documents
• Lead execution of equipment cleaning validations
• Support equipment cleaning harmonization and continuously develop the cleaning validation process (procedures, templates, R&R) in collaboration with site and global functions
• Keep up to speed with regulations and their implementation on site if applicable, development of risk based approaches to cleaning validation
• Work closely with Operations and Quality to ensure smooth delivery of work packages

Key Requirements:

• Master's degree preferred, or Bachelor's Degree plus relevant industry experience. Area of study in Biotechnology or similar science related field.
• Intermediate previous experience working in the biotech industry
• Intermediate GMP experience
• Very good planning and organizing skills, including risk management skills
• Fluent in English

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.