- Location
- CH - Visp, Switzerland
- Type
- Full-time
- Department
- Education
- Source
- Workday
Description
The actual location of this job is in Visp, Switzerland.
This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards
Responsible for the technical and GMP-compliant management of analytical equipment within QC throughout its entire lifecycle – from procurement and qualification through routine operation, maintenance and ultimately decommissioning.
The position ensures that QC equipment remains qualified, available, compliant with applicable requirements, and fit for its intended purpose at all times.
What you will get:
An agile career and a dynamic work culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
What you will do:
Manage the complete lifecycle of QC analytical equipment, from user requirements and qualification through routine operation and decommissioning
Coordinate equipment procurement, installation, maintenance, calibration, qualification, and replacement activities
Prepare, review, and support IQ/OQ/PQ documentation and ensure GMP-compliant execution of qualification activities
Investigate equipment-related deviations, support change controls and CAPAs, and contribute to risk assessments
Coordinate vendors and service providers during installation, qualification, maintenance, and repair activities
Support QC teams in troubleshooting technical issues and implementing sustainable corrective actions
Participate in equipment and infrastructure projects while driving continuous improvement initiatives
What we are looking for:
Completed university/college degree in Chemistry, Pharmacy, Biotechnology, Process Engineering or a comparable scientific or technical discipline or a comparable qualification (e.g. laboratory technician) combined with relevant professional experience)
Experience working in a GMP-regulated environment, ideally within the pharmaceutical or biotechnology industry
Knowledge of analytical laboratory equipment and equipment qualification processes
Understanding of IQ/OQ/PQ requirements and GMP documentation standards
Experience managing deviations, change controls, and CAPAs
Strong problem-solving, communication, and stakeholder management skills
Fluency in German and English
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.