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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...Qualität
- ...or Technology; or equivalent professional experience. ? 1-3 years of experience in a GMP regulated environment, preferably within Quality Systems, Documentation, or Digital Quality ? Hands on experience with Veeva Knowledge or similar electronic document / knowledge...Qualität
- ...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...Qualität
- ...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...QualitätVollzeit
- ...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)....QualitätVollzeit
- ...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...Qualität
- ...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...QualitätHomeoffice
- ...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...Qualität
- ...delivering tailored solutions that create real business value. Drives delivery excellence , holding ourselves accountable for the quality and impact of every outcome. Encourages entrepreneurial thinking , empowering you to take initiative, solve problems, and lead...QualitätVollzeit