Senior Scientist QC 80%-100% (m/f/d)
Lonza Group
- Employment type
- Part-time
- Location
- Visp
- First posted
Location: Visp (Switzerland) Relocation assistance is available for eligible candidates and their families. Lonza is today a world-leading company in the Life Sciences sector, operating on three continents. We work in science, but there is no magic formula for how we approach our 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, big and small, improve the world. And that's the kind of work we want to be a part of. For our Visp site, we are looking for a Senior Scientist QC. As a member of the Biologics Quality Control team, you will be responsible for release analytics of a wide range of analytical methods in the analysis of biopharmaceutical molecules for clinical and commercial use, while adhering to quality and safety guidelines. You will work independently within the scope of projects and take on responsibility, maintaining close contact with other QC groups, research, production, and quality assurance. What we offer: An agile career and dynamic work culture An integrative 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 expense allowances, and subsidized meals. Your tasks: Implementation, optimization, transfer, and validation of analytical methods, with a focus on HPLC analytics Planning and co-responsibility for the execution of release analytics Technical expertise in technical and analytical issues Extraction and evaluation of analytical data as well as preparation of reports and presentations Processing of investigations, change requests, and deviations under cGMP Creation, review, and approval of documents to ensure compliance with regulatory guidelines Leadership of innovation projects Representative for project-specific inquiries in audits and inspections Standby service with previously agreed-upon deployments as part of the on-call service Your profile: You have a completed degree (FH/BSc/MSc/Diplom) in the field of biochemistry, biology, or chemistry. You ideally have professional experience in the field of quality control and are familiar with the corresponding processes under GMP and/or in the analysis of large bio-molecules. You are independent, responsible, and possess good communication and team skills as well as a willingness to work in an interdisciplinary team. You enjoy contributing to a young, dynamic team, are committed, and have initiative. Secure German and English skills round out your profile. Lonza's products and services have a positive impact on millions of people every day. For us, this is 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 paramount, and we protect both our employees and the environment. Success for us means morally justifiable progress. People come to Lonza who take on challenges and develop new ideas in the Life Science sector with their creativity to solve complex problems. Together, we make a contribution that can improve the lives of many people around the world. This gives them the certainty and satisfaction of really making a difference with their own work.
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Posted 2 days ago