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PbLocation: /b the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /ppThis role offers the opportunity to lead and shape a comprehensive contamination control strategy within a GMP-regulated bioconjugates environment, directly impacting product quality and patient safety. You will drive cross-functional collaboration, leverage contamination control expertise, and influence continuous improvement initiatives to strengthen compliance and operational excellence. /ppbWhat you will get: /b /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 /plipLead the Bioconjugates contamination control strategy, ensuring end to end compliance across Bioconjugates manufacturing facilities. /p /lilipLead CCS-related topics, such as bioburden control strategy, hygiene, environmental monitoring, etc (managing Risk and Gap Assessments, Change Requests, Deviations, Investigations, CAPAs, etc.) in Bioconjugates. /p /lilipAuthor and approve GMP documentation and records, including: SOPs, deviations, change controls, and risk assessments /p /lilipPartner closely with cross‑functional teams to identify risks, drive deviation management continuous improvement, and strengthen contamination prevention control practices. /p /lilipLead the identification, assessment, and mitigation of contamination risks and maintaining the Contamination Control Strategy (CCS) within Bioconjugates. /p /lilipGuide and influence stakeholders by providing microbiology and QA expertise, ensuring robust quality culture and operational compliance. /p /lilipAct as QA Microbial Contamination Control and cleaning SME in meetings with the relevant stakeholders, and customers, in audits and inspections. /p /lilipReview and approving the routine cleaning-relevant documents, i.e., routine cleaning plans and reports, MAC plans and cleaning QC plans. /p /lilipResponsible for the review and final release of records like Standard Operating Procedures (SOPs), Master Batch Records, Material Specifications, Deviations, Change Requests, Effectiveness Checks, Testing Protocols Reports etc. /p /lilipIdentify emerging QA relevant topics, communicating to the relevant stakeholders and working actively on their development into new or already established Quality and Compliance strategies and/or standards i.e., CAPAs. /p /lilipSupport continuous improvement programs to establish effective Quality Contamination Control. /p /lippbbWhat we are looking for: /b /b /p /plipAcademic degree in Chemistry/Biotechnology/ Life Science or related field. /p /lilipExtensive experience in the GMP-regulated pharmaceutical industry; experience in microbial contamination control and Environmental Monitoring programs with practical understanding is required. /p /lilipGeneral knowledge of manufacturing processes, contamination control strategy, cleaning procedures and analytical methods. /p /lilipDemonstrated ability to act proactively with a detail‑oriented, problem‑solving and continuous‑improvement mindset. /p /lilipExperience in the interaction with health authorities (Swissmedic, FDA etc.) is desired. /p /lilipWe are looking for someone who is independent, sociable, pro-active, customer focused and who values working as a tea m player. /p /lilipExperience with TrackWise, SAP, and Microsoft Office software is preferred. /p /lilipFluency in English is required; German would be an asset. /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: R76189
