ph3bEquipment Engineer - Small Devices /b /h3pEnsure the operational readiness and reliability of vital small manufacturing equipment at our BioAtrium facility in Visp, directly supporting the delivery of life-changing biopharmaceuticals. This is a fully site-based 6-month contract role. /ph3bFully site‑based roles /b /h3pThis 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. /ppbWhat you will get: /b /pulliAn agile career and dynamic working culture. /liliAn inclusive and ethical workplace. /li /ulpbWhat you will do: /b /pulliDrive equipment lifecycle management and reliability for small utility and process devices across the BioAtrium site. /liliSupport the continuous production of biopharmaceuticals by minimizing equipment downtime through proactive preventive and corrective maintenance. /liliServe as the Subject Matter Expert (SME) on CAPEX projects, contributing to equipment design, selection, procurement, installation, and commissioning. /liliCollaborate closely with cross-functional teams including Engineering, Operations, Quality, and Validation to maintain operational excellence. /liliTroubleshoot complex equipment deviations using structured Root Cause Analysis (RCA) and implement effective CAPAs. /liliAuthor, review, and manage critical cGMP documentation, including SOPs, work instructions, change controls, and investigation reports. /liliRepresent the engineering department during internal and external audits, ensuring complete audit readiness for small device systems. /li /ulpbWhat we are looking for: /b /pulliMinimum 10 years of professional engineering experience, with at least 3 years in a cGMP pharmaceutical or biotechnology manufacturing environment. /liliProven expertise in equipment lifecycle management, reliability engineering, and maintenance optimization. /liliHands‑on experience with equipment commissioning, qualification, and validation (CQV/Validation: IV, IQ/OQ/PQ) and risk assessments. /liliDemonstrated track record in technical troubleshooting and Root Cause Analysis (RCA); formal RCA certification is an advantage. /liliStrong proficiency in authoring and managing GMP quality records (deviations, CAPAs, change controls). /liliProfessional fluency in English (written and spoken); working knowledge of German is an advantage. /liliDegree in Engineering (Mechanical, Process, Chemical, or related technical discipline). /li /ulh3bAbout Lonza /b /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. /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. /p /p #J-18808-Ljbffr
Equipment Engineer in Raron Arbeitgeber: Lonza Group AG
Lonza ist ein hervorragender Arbeitgeber, der eine dynamische Arbeitskultur und agile Karrieremöglichkeiten in einem hochmodernen biopharmazeutischen Umfeld bietet. In Visp, Schweiz, profitieren Mitarbeiter von einer engen Zusammenarbeit vor Ort, die es ermöglicht, qualitativ hochwertige und sichere Medikamente herzustellen. Wir fördern Vielfalt und Inklusion und bieten unseren Mitarbeitern die Möglichkeit, ihre Fähigkeiten weiterzuentwickeln und einen direkten Einfluss auf die Lebensqualität der Menschen zu haben.
