Relocation assistance is available for eligible candidates and their families, if needed.

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 Junior CSV Engineer in the Biologics division, you will support the validation of computerized systems on process engineering equipment and facilities. Working closely with the CQV (Commissioning, Qualification, and Validation) team, you will gain hands-on experience in planning and executing qualification and validation activities that arise from projects and system changes throughout the system life cycle. You will learn how to ensure compliance with regulatory standards, contributing to the ongoing optimization of processes, systems, and internal procedures. Additionally, you will develop the technical knowledge necessary to support plant personnel and engineering teams in sustaining the quality and reliability of our biologics production environment.

What you will get

• Agile career and dynamic work culture – grow in a flexible and innovative environment.

• Inclusive and ethical workplace – we value diversity, integrity, and collaboration.

• Attractive compensation and benefits – in addition to a competitive salary, enjoy numerous lifestyle, family, and leisure perks. Full details for Visp can be found here: Benefits in Visp.

What you will do

• Document Preparation: Assist in preparing commissioning and validation documents for new and existing systems in compliance with GEP and GMP.

• Project Support: Participate in CSV activities for new constructions, system upgrades, and post-go-live life cycle support.

• Deviation and Change Management: Support the review of deviations, change controls, and CAPAs to ensure compliance.

• CSV Coordination: Collaborate with internal teams and external providers to coordinate CSV tasks and timelines.

• Audit Support: Assist in preparing CSV documentation for audits and inspections.

• Scheduling and Reporting: Track CSV activity schedules and compile progress reports.

• QA Alignment: Support alignment of CSV activities with the QA strategy for Biologics.

• Document Improvement: Contribute to reviewing and improving CSV documents to meet quality standards.

• Other Duties: Perform additional tasks as required.

What we are looking for

• Bachelor’s, Master’s, or Diploma from a technical school (HF), university of applied sciences (FH), or university in a technical field.

• Experience in a regulated environment, particularly in Computerized System Validation (CSV).

• Proficiency in Microsoft Office.

• Knowledge of KNEAT, COMOS (plant engineering software), DMS, TrackWise, and SAP is an advantage.

• Fluent in English; German language skills are a plus.

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.

Ready to shape the future of life sciences? Apply now.