Lonza AG
Manufacturing Specialist
📍 CH - Visp
Role and responsibilities
Perform upstream or downstream manufacturing activities following cGMP guidelines. Troubleshoot equipment, evaluate test results, and recommend solutions. Support safety, environmental monitoring, and cleaning risk assessments. Prepare and maintain documentation such as batch records and SOPs. Review production documents and support deviations, change requests, and CAPAs. Contribute to capital investment projects and equipment commissioning. Train manufacturing staff on equipment and standard operations.
Team / description
Today, Lonza is a global leader in life sciences operating across five continents. 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.
Qualifications and Skills
Education or training in Biotechnology, Biology, Biochemical Engineering, or related field
Experience in microbial or mammalian cultivation, or protein purification
Strong communication skills and a collaborative mindset
Fluent in English; German is a plus
Willingness to work in a 4-shift system
Basic understanding of GMP is an advantage