Customer Audit Manager / Senior QA Specialist 80-100% (f/m/d) in Raron

pLocation: Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /ppFor our site in Visp we are looking for a Senior QA Specialist /Customer Audit Manager (f/m/d) with a strong scientific background and experience in GMP manufacturing. He/She is responsible for the planning, execution and documentation of all customer audits and for the management of internal audits (self-inspections) and paper inspections by regulatory authorities. The Audit Manager also supports the QA Management in the preparation, execution and documentation of on-site regulatory inspections. The Audit Manager has face-to-face contact with Lonza’s customers on a regular basis and is therefore a key person for Lonza’s business. /ph3What you will get /h3ulliAn agile career and dynamic working culture /liliAn inclusive and ethical workplace /liliCompensation programs that recognize high performance /liliA variety of benefits dependant on role and location /liliThe full list of our global benefits can be also found on /li /ulh3What you will do /h3ulliPlanning, executing and documenting customer audits on the Visp site /liliResponding to customer requests for audit dates /liliPlanning audits together with Lonza project teams, based on the customers’ agendas /liliAccompanying the customer throughout the audit (plant tours, documentation review etc.) /liliPresenting Lonza’s Quality systems to the customer /liliDocumenting the customer audits in TrackWise /liliCoordinating the responses to audit observations with the project team and ensuring that the customer receives the responses within the given timelines /liliProviding KPI data to QA Management on a regular basis /liliConducting internal audits (self-inspections) /liliScheduling, preparing and performing internal audits as per approved audit schedule /liliAgree on an appropriate CAPAs and monitor the implementation to a satisfactory conclusion /liliSupporting QA management during regulatory inspections /liliOrganizing of preparation meetings and SME trainings /liliSupport in Front Office/Back Office as required /liliResponsible for QA aspects of paper inspections /liliCoordinating with Regulator Affairs to provide all required documents /liliAnswering queries from regulatory authorities with respect to paper inspections /li /ulh3What we are looking for /h3ulliAcademic degree in Chemistry/ Biotechnology/ Life Sciences etc /liliExcellent communication skills in English and German (fluency in both languages is required) /liliProfessional appearance and attitude to establish and maintain excellent working relationship with customers /liliExcellent verbal, written and interpersonal communications skills /liliExcellent organizational skills /liliAbility to work in partnership as an active member of a team and/or cross functional working groups /liliAbility to prioritize and manage work to meet timelines in a fast-paced environment /liliGeneral knowledge of manufacturing processes and analytical methods /liliCompetent level of general IT skill (e.g. MS Office) is required /liliExperience in auditing chemical/biopharmaceutical processes is an asset /li /ulh3About Lonza /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. /ppOur 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. /ppAt Lonza, we value diversity and are committed to creating an inclusive environment for all employees. /ppIf you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. /p #J-18808-Ljbffr