pThe actual location of this job is in Visp, Switzerland. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards Responsible for the technical and GMP‑compliant management of analytical equipment within QC throughout its entire lifecycle – from procurement and qualification through routine operation, maintenance and ultimately decommissioning. The position ensures that QC equipment remains qualified, available, compliant with applicable requirements, and fit for its intended purpose at all times. /ph3What you will get: /h3ulliAn agile career and a dynamic work culture /liliAn inclusive and ethical workplace /liliCompensation programs that recognize high performance /li /ulh3What you will do: /h3ulliManage the complete lifecycle of QC analytical equipment, from user requirements and qualification through routine operation and decommissioning /liliCoordinate equipment procurement, installation, maintenance, calibration, qualification, and replacement activities /liliPrepare, review, and support IQ/OQ/PQ documentation and ensure GMP‑compliant execution of qualification activities /liliInvestigate equipment‑related deviations, support change controls and CAPAs, and contribute to risk assessments /liliCoordinate vendors and service providers during installation, qualification, maintenance, and repair activities /liliSupport QC teams in troubleshooting technical issues and implementing sustainable corrective actions /liliParticipate in equipment and infrastructure projects while driving continuous improvement initiatives /li /ulh3What we are looking for: /h3ulliCompleted university/college degree in Chemistry, Pharmacy, Biotechnology, Process Engineering or a comparable scientific or technical discipline or a comparable qualification (e.g. laboratory technician) combined with relevant professional experience) /liliExperience working in a GMP‑regulated environment, ideally within the pharmaceutical or biotechnology industry /liliKnowledge of analytical laboratory equipment and equipment qualification processes /liliUnderstanding of IQ/OQ/PQ requirements and GMP documentation standards /liliExperience managing deviations, change controls, and CAPAs /liliStrong problem‑solving, communication, and stakeholder management skills /liliFluency in German and English /li /ulh3About Lonza /h3pAt Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. /ppReady to shape the future of life sciences? /ppEvery day, our teams across the world work together to turn scientific breakthroughs into life‑changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong. You will feel at home at Lonza if you: /pulliTake ownership, step forward, and enjoy meaningful responsibility /liliLove solving problems and thrive in a complex, fast‑moving environment /liliAre curious, always looking to learn and improve /liliWork collaboratively, contributing to something bigger than yourself /liliAre motivated to make a difference through work that impacts customers and their patients /li /ulh3Why Lonza /h3pWe are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow. Join us. Be you. /p #J-18808-Ljbffr
Scientist QC Equipment & Qualification 80-100% (f/m/d) in Raron Arbeitgeber: Lonza Group Ltd.
Die Lonza Group Ltd. ist ein hervorragender Arbeitgeber, der seinen Mitarbeitenden in der Region Oberwallis nicht nur ein wettbewerbsfähiges Gehalt, sondern auch ein unterstützendes und innovatives Arbeitsumfeld bietet. Unsere Unternehmenskultur fördert die persönliche und berufliche Weiterentwicklung, während wir gleichzeitig großen Wert auf Sicherheit und Teamarbeit legen. Als Werkstattleiter haben Sie die Möglichkeit, Prozesse zu optimieren und Ihr Team aktiv zu führen, was Ihnen eine bedeutende Rolle in unserem Unternehmen verleiht.
