CSV Engineer 80-100% (m/f/d)

ppSwitzerland, Visp /ppRelocation assistance is available for eligible candidates and their families, if needed. /ppAs a CSV Engineer (m/f/d) you will be responsible for the generation and execution of the validation of the computerized systems on process engineering equipment and facilities, including MES. You are responsible to follow the planning and implementation of CSV activities resulting from projects and plant adaptations during the system life cycle of the plants, as well as make a contribution to the ongoing optimization of processes, facilities and internal procedures. /ppThis role is primarily based on site. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. /ph3What You’ll Get /h3ulliAn agile career and dynamic working culture. /liliAn inclusive and ethical workplace. /liliCompensation programs that recognize high performance. /liliIn addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits in Visp can be found on 9cd58bc563c44174b5a4f5fedd /li /ulh3What you will do: /h3ulliPrepare commissioning and validation documents for new systems, and supervise conversion, expansion, and new construction projects. This includes CSV activities for critical systems in new construction projects and SLC support for all systems post debut. /liliSupervise deviations, changes (GEP and GMP), and CAPAs, ensuring strict adherence to protocols. /liliCoordinate CSV executions with internal groups, as well as external service providers and suppliers, to strictly ensure seamless integration. /liliPresent CSV documents during audits and inspections, showcasing our world‑class standards. /liliSchedule and report CSV activities, maintaining a flawless record of progress and outcomes. /liliAlign CSV strategy with QA CSV for all Biologics scope, showcasing our dedication to high standards. /liliContribute to the review and continuous amelioration of all CSV documents, ensuring ongoing optimization and success. /li /ulh3What we are looking for: /h3ulliBachelor / Master / Diploma from a technical school (HF) / university of applied sciences (FH) or university in a technical field or equivalent experience, showcasing your solid educational foundation. /liliSignificant experience in a regulated environment with regard to Computerized System Validation (CSV), demonstrating your proven expertise. /liliGood knowledge of Microsoft Office and Delta‑V, essential for your successful implementation of tasks. /liliKnowledge of KNEAT, COMOS (plant engineering software solution), DMS, TrackWise, and SAP is an advantage, improving your ability to compete in our ambitious environment. /liliProficient in English, with German language skills being advantageous, enabling you to collaborate effectively in our diverse team. /li /ulh3About Lonza /h3pAt Lonza, our people are our greatest strength. Spread across 30+ sites and 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 shape what we achieve and how we achieve it. 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 offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. /ppIf you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. /ppReference: R73839 /p /p #J-18808-Ljbffr