PpbLocation: /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. /ph3bBenefits: /b /h3pAn agile career and a dynamic work culture. /ppAn inclusive and ethical workplace. /ppCompensation programs that recognize high performance. /ppIn 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. /ppLead the Bioconjugates contamination control strategy, ensuring end to end compliance across Bioconjugates manufacturing facilities. /ppLead 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. /ppAuthor and approve GMP documentation and records, including: SOPs, deviations, change controls, and risk assessments. /ppPartner closely with cross‑functional teams to identify risks, drive deviation management continuous improvement, and strengthen contamination prevention control practices. /ppLead the identification, assessment, and mitigation of contamination risks and maintaining the Contamination Control Strategy (CCS) within Bioconjugates. /ppGuide and influence stakeholders by providing microbiology and QA expertise, ensuring robust quality culture and operational compliance. /ppAct as QA Microbial Contamination Control and cleaning SME in meetings with the relevant stakeholders, and customers, in audits and inspections. /ppReview and approving the routine cleaning‑relevant documents, i.e., routine cleaning plans and reports, MAC plans and cleaning QC plans. /ppResponsible 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. /ppIdentify 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. /ppSupport continuous improvement programs to establish effective Quality Contamination Control. /ph3bQualifications: /b /h3pAcademic degree in Chemistry/Biotechnology/ Life Science or related field. /ppExtensive experience in the GMP‑regulated pharmaceutical industry; experience in microbial contamination control and Environmental Monitoring programs with practical understanding is required. /ppGeneral knowledge of manufacturing processes, contamination control strategy, cleaning procedures and analytical methods. /ppDemonstrated ability to act proactively with a detail‑oriented, problem‑solving and continuous‑improvement mindset. /ppExperience in the interaction with health authorities (Swissmedic, FDA etc.) is desired. /ppWe are looking for someone who is independent, sociable, pro‑active, customer focused and who values working as a team player. /ppExperience with TrackWise, SAP, and Microsoft Office software is preferred. /ppFluency in English is required; German would be an asset. /p /p #J-18808-Ljbffr