ph3bProduction Engineer - Small Devices /b /h3 pEnsure 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. /p h3bFully site‑based roles /b /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 pbWhat you will get: /b /p ulliAn agile career and dynamic working culture. /liliAn inclusive and ethical workplace. /li /ul pbWhat you will do: /b /p ulliDrive equipment lifecycle management and reliability for small utility and process devices across the BioAtrium site. /li liSupport the continuous production of biopharmaceuticals by minimizing equipment downtime through proactive preventive and corrective maintenance. /li liServe as the Subject Matter Expert (SME) on CAPEX projects, contributing to equipment design, selection, procurement, installation, and commissioning. /li liCollaborate closely with cross-functional teams including Engineering, Operations, Quality, and Validation to maintain operational excellence. /li liTroubleshoot complex equipment deviations using structured Root Cause Analysis (RCA) and implement effective CAPAs. /li liAuthor, review, and manage critical cGMP documentation, including SOPs, work instructions, change controls, and investigation reports. /li liRepresent the engineering department during internal and external audits, ensuring complete audit readiness for small device systems. /li /ul pbWhat we are looking for: /b /p ulliMinimum 10 years of professional engineering experience, with at least 3 years in a cGMP pharmaceutical or biotechnology manufacturing environment. /li liProven expertise in equipment lifecycle management, reliability engineering, and maintenance optimization. /li liHands‑on experience with equipment commissioning, qualification, and validation (CQV/Validation: IV, IQ/OQ/PQ) and risk assessments. /li liDemonstrated track record in technical troubleshooting and Root Cause Analysis (RCA); formal RCA certification is an advantage. /li liStrong proficiency in authoring and managing GMP quality records (deviations, CAPAs, change controls). /li liProfessional fluency in English (written and spoken); working knowledge of German is an advantage. /li liDegree in Engineering (Mechanical, Process, Chemical, or related technical discipline). /li /ul h3bAbout Lonza /b /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. /p pAs Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role. /p /p #J-18808-Ljbffr
Production 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.
