StellenbeschreibungpbLocation: /b the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /ppWe are looking for a (Senior) QA Specialist Qualification (f/m/d), who will support our team QA Plant Qualification. /pppbbWhat you will get: /b /b /p /plipAn agile career and a dynamic work culture. /p /lilipAn inclusive and ethical workplace. /p /lilipCompensation programs that recognize high performance. /p /lipIn addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below. /ppBenefits in Visp: /pppbbWhat you will do: /b /b /p /plipRepresentative of QA Qualification in the project organization for new facilities or other projects in regard to qualification of facilities, utilities, equipment and systems /p /lilipCoordinating different QA interests during the project phase e.g. process, cleaning or other relevant QA objectives /p /lilipDriving implementation of new qualification strategy and being a strong decision maker when needed /p /lilipCompiling, reviewing and releasing Qualification Documents (URS, Qualification Plan Report, DQ/IQ/OQ/PQ Reports and more) as also supporting and approving quality risk analysis (e.g. FMEA) /p /lilipPerforming assessments and approvals of technical changes requests during the different phases of a project and lifecycle and their relevance to the qualification of facilities, equipment, utilities and systems /p /lilipRepresenting qualification topics during customer audits and regulatory inspections /p /lilipBeing responsible to drive CAPA and Effectiveness Checks items to completion and timely closing as well ensuring deviations are appropriately investigated and recorded in Deviation Reports /p /lippbbWhat we are looking for: /b /b /p /plipAcademic degree in Engineering/ Chemistry/ Biotechnology or any related field /p /lilipSignificant experience in the pharmaceutical industry, ideally in a QA role /p /lilipGood understanding of the applicable cGMP regulations would be an advantage /p /lilipGeneral knowledge of engineering and manufacturing processes /p /lilipAbility to oversee project execution to identify non-compliance from quality standards /p /lilipFluent German (writtenverbal) is required; good English language skills are an advantage /p /lipbAbout Lonza /b /ppAt 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 for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. /ppbReady to shape the future of life sciences? Apply now. /b /p Reference: R77588
