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Lonza in Switzerland seeks a senior life sciences professional to author and review GMP reference standard qualification protocols and reports. You will liaise between QC customers and CSM, ensuring timely documentation of LIMS/LES activities, and provide SME input during audits.
You will mentor colleagues, lead cost- and efficiency-focused projects, and maintain data integrity across Trackwise records while collaborating with QA Analytics and external clients.
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.