Today, Lonza is a global leader in life sciences operating across three 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.
As a Senior CSV Engineer, Biologics (m/f/d) you will be responsible for the generation and execution of the validation of the computerized systems on process engineering equipment and facilities, including MES. You are responsible to follow the planning and implementation of CSV activities resulting from projects and plant adaptations during the system life cycle of the plants, as well as contribute to the ongoing optimization of processes, facilities and internal procedures.

• Preparation of commissioning and validation documents for new systems, as well as the supervision of conversion, expansion and new construction projects. This is broken down into CSV activities on new construction projects for critical systems and SLC support for all systems after going live.
• Supervising the junior CSV Engineers including training and coaching.
• Supervision of deviations, changes (GEP and GMP), and CAPAs, as well as review and amelioration of all CSV documents (SOPs, and executables).
• Coordination of CSV executions with internal groups in the Biologics division, as well as external service providers and suppliers.
• Responsible for the presentation of CSV documents during audits and inspections.
• Scheduling and reporting of CSV activities.
• Following the alignment of the CSV strategy with the QA CSV for all Biologics scope.