Project Leader Quality Control for Drug Product (m/f/d)

Lonza AG

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  • Publication date:

    08 March 2024
  • Workload:

    100%
  • Contract type:

    Permanent position
  • Place of work:

    Visp

Project Leader Quality Control for Drug Product (m/f/d)

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.

We are currently looking for a Project Leader Quality Control (m/f/d) for Drug Product in Visp.

Key responsibilities:

  • Within the matrix organization of the project team, you are in close contact with the analytical laboratories as well as with the program management, process development, production, and quality assurance departments, among others

  • Through excellent planning and management of the project, you will ensure timely and cost-effective processing of orders, even in the face of changing customer requirements and priorities

  • Establish and maintain customer relationships

  • Preparation and supervision of production batches including sample distribution

  • Processing of change requests and deviations under GMP

  • Supervision of customer audits and inspections by authorities

  • Calculating and monitoring QC costs in the project

Key requirements:

  • Doctoral or master degree in microbiology, biology, biotechnology or related field with significant experience in a biopharmaceutical environment

  • Practical experience and scientific expertise in drug product relevant areas

  • Able to analyze and solve complex problems that do not have routine solutions

  • Strong team orientation, structured, solution-oriented and well-organized working attitude

  • Strong project management skills

  • Fluency in English is required, German is a plus

  • Experience with method validation and technology transfer preferred

  • Knowledge of SAP, TrackWise and LIMS systems is a plus

  • GMP experience (desirable)

  • Multiple years’ of experience in aseptic processing for Drug Product and associated installations e.g. filling line / isolator / depyrogenation tunnel / lyophilizer etc. (desirable)

  • Media Fill / Aseptic Process Simulation experience (desirable)

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.

Reference: R59124

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