ppJoin Lonza in Visp as a Quality Control Expert on a 7-month contract. Lead and streamline analytical deliverables for Drug Product operations while managing key client relationships in a fully site-based setting. /p h3Fully site-based roles /h3 pThis 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. /p h3What you will get: /h3 ul liAn agile career and dynamic working culture. /li liAn inclusive and ethical workplace. /li /ul h3What you will do: /h3 ul liDrive high-impact Drug Product (DP) programs by acting as the primary QC lead across the entire product lifecycle. /li liServe as the vital link between internal laboratories, cross-functional teams, and global pharmaceutical clients. /li liSynchronize critical analytical deliverables, including method validation, analytical transfers, stability testing, and final batch release. /li liOversee milestone delivery and proactively mitigate technical or scheduling risks to maintain strict regulatory compliance. /li liMaintain transparent project governance through structured status reporting and alignment meetings. /li liFoster professional growth across teams through collaborative problem-solving and mentoring cross-functional peers. /li liSupport operational excellence initiatives to standardize processes and optimize laboratory service delivery. /li /ul h3What we are looking for: /h3 ul liProven experience within a GMP-regulated pharmaceutical environment, ideally focused on Drug Product manufacturing or testing workflows. /li liStrong technical background in core Quality Control processes and laboratory operations. /li liDemonstrated ability to coordinate complex projects or lead cross-functional initiatives under tight timelines. /li liOutstanding communication and negotiation skills to manage diverse client and internal stakeholder expectations. /li liA proactive, solution-oriented mindset suited for a fast-paced manufacturing site. /li liUniversity degree (B.Sc., M.Sc., or Ph.D.) in Pharmaceutical Sciences, Chemistry, Biotechnology, or a related Life Sciences field. /li /ul 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. /p pAt Lonza, we value diversity and are committed to creating an inclusive environment. /p /p #J-18808-Ljbffr
Quality Control Expert 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.
