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- ...Title: Quality Specialist Location: Visp, Valais, Switzerland (On-site) We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related...Qualità
- ...you will support CAPEX projects through operational procurement activities and work closely with Engineering, Project Management, Quality, and Finance teams. Your Responsibilities Support operational procurement activities within CAPEX projects Prepare and manage...Qualità
- ...Lonza Visp, Switzerland The Senior Scientist in Quality Control serves as a scientific and strategic leader within the QC organization. In this role, you will oversee complex analytical projects, drive method development and validation activities, and ensure...Qualità
- ...deliver customer programs across their full lifecycle - from technology transfer to GMP manufacturing and project closure - ensuring quality, timelines, and cost-effectiveness. Act as a trusted partner and main point of contact for customers, fostering transparent...Qualità
- ...Visp, Switzerland In this senior MSAT role based in Visp, Switzerland, you will play a key part in safeguarding product quality and patient safety by driving risk‑based impurity compliance for Small Molecules. You will lead impurity risk assessments and shape...Qualità
- ...facilities, ensuring compliance with cGMP requirements and industry regulations. You will collaborate closely with engineering, quality, and operations teams to ensure that equipment and infrastructure are installed, tested, and validated according to regulatory and...QualitàTempo pieno
- ...laboratory work, driving upstream development activities and collaborating with cross-functional teams and customers to deliver high-quality bioprocessing solutions. Key responsibilities: Lead, design, and execute complex upstream process development...Qualità
- ...cause analyses and track CAPAs Initiate and manage change requests (CRs) Ensure timely closure of deviations in line with quality system requirements Identify and implement improvement measures to harmonize hygiene processes across production areas Support...Qualità
- ...gap analyses and continuous improvement across the validation lifecycle; apply lessons learned and regulatory updates. Perform Quality Systems activities: Document Management, Change Control, Non-conformities/Deviations, CAPA; write/revise procedures (SOPs/WIs)....QualitàTempo pieno
- ...SRM): Develop relationship plans with key partners, manage strategic key accounts, and evaluate new suppliers to ensure capacity and quality. Project Management: Act as a core member of the Global Category Team for Construction, Fit-out, and Automation. Maintain weekly...QualitàHome office
- ...Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece. If you can stare down a regulatory inspector with a calm smile and a...Qualità
- ...learned. Monitor regulatory expectations; implement updates to keep programs aligned with cGMP/Annex 15 and internal SOPs. Support Quality Systems activities: Document Management, Change Control, Deviations/Non-conformities, and CAPAs. Collaborate cross-functionally...Qualità