(Senior) Scientist - Bioconjugates (all genders) 80%-100%

Location: Visp (Switzerland) If required, relocation support is available for eligible candidates and their families. Lonza is today a leading global company in the field of Life Sciences, operating on three continents. We work in science, but there is no magic formula for how we approach the work. Our most important scientific solution is talented employees who collaborate and develop ideas that help other companies help people. In return, our employees steer their careers independently. Because their ideas, whether big or small, improve the world. And that is the kind of work we want to be part of. As a member of Quality Control (QC), you are responsible for the practical execution of a wide range of biochemical methods for the characterization of complex and highly active conjugated antibody drug products (as well as other biomolecules) under GMP. Bioconjugates are an innovative class of active ingredients in which great hopes are placed, including in cancer therapy. The Biochemistry Team works predominantly with bioconjugates and belongs to the QC-Biology department. To strengthen our laboratory team, we are looking for a Junior Scientist. What we offer you: An agile career and a dynamic work culture; An inclusive and ethical workplace; Compensation programs that recognize high performance. In addition to competitive salaries, you will find a wide range of lifestyle, family, and leisure benefits. Depending on the location, these benefits may include family allowances, childcare support, discounts for local businesses and attractions, travel allowances, and subsidized meals. Your tasks: Independent application of biochemical analytical methods with a focus on ELISA, gel electrophoresis, and rDNA analytics. Participation in method development, implementation, transfer, and validation, as well as the evaluation of data and solving analytical questions - particularly in the area of cell-based assays. Planning, coordination, and execution of release tests as well as technical support for analytical and technical questions in the GMP environment. Independent processing of deviations, change requests, and investigations within the framework of regulatory requirements. Evaluation and interpretation of analytical data as well as the creation of scientific reports and presentations. Writing, checking, and releasing quality-relevant documents to ensure compliance with legal and internal specifications. Independent execution of assigned tasks within the framework of studies and projects with a focus on quality, safety, and adherence to deadlines. Your requirement profile: Completed scientific studies (BSc or higher) in biology, biochemistry, chemistry, or a related field; Ideally initial professional experience in quality control or analytics of biopharmaceuticals, preferably in a regulated GMP environment; Independent, structured, and solution-oriented way of working; Taking on responsibility and actively contributing technical expertise to the team; High quality awareness, initiative, and commitment; Very good German skills in spoken and written form as well as good English skills. Lonza's products and services have a positive impact on millions of people every day. For us, this represents not only a great honor but also a great responsibility. How we achieve our business results is just as important to us as our successes themselves. At Lonza, respect is a priority and we protect both our employees and our environment. Success for us means morally justifiable progress. People come to Lonza who accept challenges and use their creativity in the field of Life Science to develop new ideas for complex problems. Together, we make a contribution that can improve the lives of many people around the world. This offers them the certainty and satisfaction of truly making a difference with their own work.