Stability Coordinator 80-100% (m/f/d)

  • Full Time
  • Basel, Basel, Switzerland
  • TBD USD / Year
  • Lonza profile




  • Job applications may no longer being accepted for this opportunity.


Lonza

Switzerland, Basel

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.

For DPS (Drug Product Services) in Basel Switzerland, we have an open position for a Stability Coordinator in our growing team. Working closely with Analytical and Formulation Development, this team offers specialized services solutions for customers. Become part of this exciting opportunity by applying for the position of Stability Coordinator, DPS.

Key Responsibilities

  • Perform all pull activities for stability studies. Prepare documents needed for the pull. Login and receive samples in LIMS. Close collaboration with different departments.
  • Prepare documentation needed for the staging, Collect data in iLab system, Organize storage of boxes in stability chamber in close collaboration with different departments
  • Ensure receipt of stand-alone samples and stability samples including the shipping documentation and datalogger readout
  • Provides support for other sample management tasks (internal and external sample shipment, sample destruction, archiving, instrument responsibility)
  • Supports the continuous revision and optimization of the sample management process
  • Ensure safety and health protection by following lab and safety instructions and all cGMP regulations
  • Perform other duties as assigned.

Required Qualifications And Skills

  • Completed apprenticeship in Life Sciences or a related field
  • Some experience in the pharmaceutical or chemical industry, preferably in sample management
  • Excellent working knowledge and solid experience working in a GMP environment and experience and understanding of ICH stability guidelines
  • Good working knowledge in stability testing of pharmaceuticals
  • Prior experience with QC stability and sample management and LIMS
  • Good working knowledge in biotechnology development processes
  • Excellent reporting and scientific skills
  • Excellent knowledge of written and spoken English

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: R56704

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To apply for this job please visit www.lonza.com.


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