pbLocation: /bthe actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /ppThe site in Visp, Switzerland is growing and for our Biologics Quality organization, we are currently looking for a Senior QA Specialist (f/m/d) for the Bioconjugates plant. The successful candidate will be responsible for QA Bioconjugates activities and will be in direct contact with the key stakeholders in the Operations Team, MSAT, QA/QC Project Management teams within the organization. /ppbWhat you will get: /b /pulliAn agile career and dynamic working culture /liliAn inclusive and ethical workplace /liliCompensation programs that recognize high performance /liliA variety of benefits dependant on role and location /liliSupport continuous improvement programs to establish effective Quality Management System in Bioconjugates. /liliPartner closely with cross‑functional teams to identify risks, drive deviation management continuous improvement. /liliGuide and influence stakeholders by providing QA expertise, ensuring robust quality culture and operational compliance. /liliManage and actively participate in “QA on the floor” program, including QA walkdowns and GEMBA walks. /liliAct as QA SME in meetings with the relevant stakeholders, and customers, in audits and inspections. /liliResponsible for the review and final release of records like Standard Operating Procedures (SOPs), Deviations, Change Requests, Effectiveness Checks, risk assessment etc. /liliIdentify emerging QA relevant topics, communicating to the relevant stakeholders and working actively on their development into new or already established Quality and Compliance strategies and/or standards i.e., CAPAs. /liliTrain and coach new employees and existing QA Specialists. /li /ulh3bWhat we are looking for: /b /h3ulliAcademic degree in Chemistry/ Biotechnology/ Life Science or related field. /liliExtensive experience in the GMP-regulated pharmaceutical industry including continuous improvement within QA area required. /liliGreen Belt certification is an advantage. /liliGeneral knowledge of manufacturing processes, great understanding and knowledge in Deviations, CAPA and Change Request management including related activities. /liliDemonstrated ability to act proactively with a detail‑oriented, problem‑solving and continuous‑improvement mindset. /liliWrite, review and approve documents e.g. SOPs and other Quality documents as applicable /liliExperience in the interaction with health authorities (Swissmedic, FDA etc.) is desired. /liliWe are looking for someone who is independent, sociable, pro-active, customer focused and who values working as a team player. /liliExperience as a QA trainer or trained as a trainer for Quality topics is an advantage. /liliExperience with TrackWise, SAP, and Microsoft Office software is preferred. /liliFluency in English is required; German would be an asset. /li /ulpbAbout Lonza /b /ppAt 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. /ppInnovation 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. /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. /ppbWe are the makers of the medicines of tomorrow. /b /p #J-18808-Ljbffr
Senior QA Specialist, Bioconjugates 80-100% (f/m/d) 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.
