ppThe actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /p pAre you looking to work in a challenging GMP-regulated environment and make a meaningful contribution to product quality through physical and physico-chemical testing? As part of our QC Physical Analytics team, you will take ownership of analytical testing, laboratory equipment, and the continuous improvement of our processes. /p h3What you will get: /h3 ul liA diverse and rewarding role in a modern laboratory environment. /li liMeaningful work with a direct impact on product quality and patient safety. /li liAccess to modern technologies and analytical techniques. /li liOpportunities for professional and personal development. /li liA collaborative team culture built on openness, respect, and mutual support. /li /ul h3What you will do: /h3 pPerform, evaluate, and document physico-chemical analyses in compliance with cGMP requirements, regulatory expectations, and internal procedures. /p pEnsure the timely and GMP-compliant execution of assigned testing activities. /p pTake responsibility for designated laboratory equipment, including calibration, qualification, and associated documentation. /p pSupport troubleshooting activities, deviation investigations, and the implementation of corrective actions. /p pActively contribute to the development and optimization of laboratory processes, analytical methods, and workflows. /p pSupport the onboarding and training of new team members and promote knowledge sharing within the team. /p pParticipate in the on-call duty rota as scheduled. /p h3What we are looking for: /h3 pCompleted apprenticeship or degree in Chemistry, Biology, Pharmaceutical Sciences, or a comparable scientific discipline. /p pInitial or several years of experience in Quality Control, ideally within a GMP-regulated pharmaceutical, biotech, or chemical manufacturing environment. /p pExperience with physical and physico-chemical analytical techniques, such as: /p ul lipH measurements /li liUV spectroscopy for protein concentration determination /li liOsmolality and conductivity measurements /li /ul pStrong quality mindset and understanding of GMP and compliance requirements. /p pStructured, independent, and solution-oriented way of working. /p pEnjoy working collaboratively and contributing to continuous improvement initiatives. /p pGood command of English and basic German skills. /p h3About Lonza /h3 pAt 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. /p pInnovation 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. /p /p #J-18808-Ljbffr
QC Associate, Analyst in Raron Arbeitgeber: Lonza
Lonza ist ein hervorragender Arbeitgeber, der eine dynamische Arbeitskultur und flexible Arbeitsmöglichkeiten bietet, um die besten Talente zu fördern. Mit einem starken Fokus auf persönliche Entwicklung und Teamarbeit ermöglicht Lonza seinen Mitarbeitern, ihre Karriere in einem bedeutenden Bereich wie der internen Revision voranzutreiben, während sie gleichzeitig zur Verbesserung von Millionen von Leben beitragen. Die enge Zusammenarbeit vor Ort fördert nicht nur den Austausch von Ideen, sondern auch die technische Präzision, die für die Herstellung von Arzneimitteln erforderlich ist.