Scientist QC Equipment & Qualification 80-100% (f/m/d)

Lonza Group Ltd.; Oberwallis; On-site; CHF 110,000 - 140,000; Full time

Benefits offered by this job

Inclusive workplace

Competitive compensation programs

Dynamic career opportunities

Job summary

Lonza Group Ltd. in Visp, Switzerland, is seeking a specialist to manage the technical and GMP-compliant lifecycle of QC analytical equipment across procurement, qualification, operation, maintenance and decommissioning.

You will coordinate installation, calibration, qualification and replacement activities, support IQ/OQ/PQ documentation, investigate deviations, CAPAs, and contribute to risk assessments while collaborating with QC teams to ensure equipment remains qualified and fit for purpose.

Qualifications

• Degree in Chemistry, Pharmacy, Biotechnology, or Process Engineering or equivalent.
• Experience in GMP-regulated pharma/biotech environments.
• Knowledge of QC analytical equipment and qualification processes (IQ/OQ/PQ).
• Experience handling deviations, change controls, and CAPAs.
• Strong problem-solving, communication, and stakeholder management.
• Fluency in German and English.

Responsibilities

• Manage lifecycle of QC analytical equipment from user requirements to decommissioning.
• Coordinate procurement, installation, maintenance, calibration, qualification, and replacement.
• Prepare, review, and support IQ/OQ/PQ documentation and GMP qualification work.
• Investigate equipment deviations and support CAPAs and risk assessments.
• Coordinate vendors and service providers during installation and maintenance.
• Support QC teams in troubleshooting and implementing corrective actions.
• Participate in equipment and infrastructure projects and drive continuous improvement.

Skills

GMP knowledge

Analytical equipment knowledge

Problem solving

Communication skills

Stakeholder management

German & English fluency

Education

Chemistry/Pharmacy/Biotechnology/Process Engineering degree

Tools

IQ/OQ/PQ documentation knowledge

Job 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?

Every day, our teams across the world work together to turn scientific breakthroughs into life‑changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong. You will feel at home at Lonza if you:

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast‑moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

Why Lonza

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow. Join us. Be you.