Global Laboratory & PAT Systems Quality Manager (f/m/d)

☞ CH12 Lonza AG

View: 147

Update day: 21-03-2024

Location: Visp Valais VS

Category: Quality Assurance / Quality Control

Industry: Human Resources Services

Position: Mid-Senior level

Job type: Full-time

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Job content

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.

This additional position is needed to build in-house capabilities for automation and digitalization initiatives; to establish and maintain an efficient, effective, compliant and sustainable global Pharmaceutical Quality System.

Key Responsibilities
  • Ensure that global QC computerized systems are implemented and maintained under validation control.
  • Conduct projects for roll-out of new systems and system changes. Act as business project manager in such projects on a global basis.
  • Drive standardization of underlying business processes across the Lonza organization.
  • Act as the liaison between IT and the lab systems user community and actively participate in the collection and formulation of user requirements for lab systems.
  • Act as project QA for QC lab systems projects.
  • Ensure the validation document packages are up to date and managed in an efficient and effective way, making use of the internal regulations and the defined risk-based approach.
  • Consult the Global Information Quality on all topics relevant to the systems.
Key Requirements
  • Bachelor / Master level or equivalent qualification in Computer Science and / or Pharmaceutical Quality sciences
  • Experience with execution and coordination of validation projects relating to GMP processes
  • Expertise in IT, IT systems validation and its application to GMP processes e.g. manufacturing process, laboratory and business systems
  • Knowledge of GMP requirements for the validation of computer systems in the pharmaceutical industry
  • Strong technical understanding and quality mindset
  • Demonstration of good problem solving abilities / techniques applied to a project
  • Fluent in English, other languages are an asset.
  • Highly interested working in a global, GMP regulated manufacturing and laboratory environment
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.
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Deadline: 05-05-2024

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