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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
- ...-ready workspaces Documentation & Compliance: Complete accurate GMP documentation for all performed tasks Follow safety, quality, and environmental procedures Participate in investigations, CAPAs, and continuous improvement initiatives Coordinate with...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
- ...Assignment in various functions within the production facilities in compliance with safety regulations and consideration of cGMP quality requirements. Recognition, interpretation and elimination of deviations Execution of production steps incl. recording and calculations...Qualità
- ...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
- ...Manpower Welcome to a leading company in the pharmaceutical manufacturing industry, recognized for its commitment to quality, compliance, and operational excellence. We offer you the opportunity to work in a highly regulated and professional environment where your...QualitàHome office
- ...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
- ...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
- ...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...QualitàTempo pieno