pLocation: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /ppYou will support the site's Data Integrity (DI) program at one of the largest biologics manufacturing sites in the world, where reliable, complete, and accurate data is essential to ensuring product quality, patient safety, regulatory compliance, and operational excellence. In this role, you will work closely with the Site Data Integrity Lead and cross-functional stakeholders to support Data Integrity governance, promote ALCOA+ principles, support continuous improvement activities, and help maintain a sustainable state of compliance across the Visp site. /ph3What you will get /h3ulliA place in an inclusive, dynamic, and passionate team, with the opportunity to contribute to the site's Data Integrity program and collaborate with cross-functional stakeholders across a diverse GMP manufacturing environment. /liliAn agile career and a dynamic work culture. /liliAn inclusive and ethical workplace. /liliCompensation programs that recognize high performance. /li /ulh3What you will do /h3ulliSupport the site's Data Integrity governance program and contribute to the implementation of DI standards, initiatives, and site-specific improvement activities. /liliPromote Data Integrity awareness and ALCOA+ principles through training programs, coaching, and engagement with site functions across Visp. /liliPlan, coordinate, and support the execution of Data Integrity Walkthroughs across the Visp site and drive follow-up actions as required. /liliSupport and coordinate Data Integrity assessments, remediation activities, and continuous improvement initiatives across GMP processes on site. /liliProvide Data Integrity support for deviations, investigations, change controls, CAPAs, quality risk assessments, audits, and inspections. /liliDeputize the Visp Data Integrity Community and act as deputy for the Site Data Integrity Lead, facilitating community meetings, stakeholder engagement, and site-wide alignment activities as required. /li /ulh3What we are looking for /h3ulliAcademic degree in Life Sciences, Engineering, Information Technology, Pharmaceutical Sciences, Quality Management, or another relevant discipline. /liliExperience in a GMP-regulated pharmaceutical, biotechnology, or healthcare environment. /liliGood understanding of Data Integrity principles, ALCOA+, computerized systems, and applicable regulatory requirements. /liliExperience with quality processes, including deviations, investigations, CAPAs, change controls, and risk assessments. /liliAbility to identify compliance risks, evaluate issues, and support the implementation of effective and pragmatic solutions. /liliStrong communication and collaboration skills with the ability to work effectively in cross-functional teams. /liliExperience supporting Data Integrity, compliance, computerized systems, CSV, Quality Systems, or related GMP activities. /liliExperience supporting audits, inspections, or regulatory interactions is desirable. /liliFluency in English is required; German is an advantage. /li /ulpEvery day, our teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year. /ppLonza is a place where people can make a unique impact, grow their careers and belong. /ph3You will feel at home at Lonza if you /h3ulliTake 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, you will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow. Join us. Be you. /p #J-18808-Ljbffr
Manager, QA, Data Integrity Program Manager in Raron Arbeitgeber: Lonza Group Ltd.
Die Lonza Group Ltd. ist ein hervorragender Arbeitgeber, der seinen Mitarbeitenden in der Region Oberwallis nicht nur ein wettbewerbsfähiges Gehalt, sondern auch ein unterstützendes und innovatives Arbeitsumfeld bietet. Unsere Unternehmenskultur fördert die persönliche und berufliche Weiterentwicklung, während wir gleichzeitig großen Wert auf Sicherheit und Teamarbeit legen. Als Werkstattleiter haben Sie die Möglichkeit, Prozesse zu optimieren und Ihr Team aktiv zu führen, was Ihnen eine bedeutende Rolle in unserem Unternehmen verleiht.
