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- ...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...Empfohlen
- ...by driving risk‑based impurity compliance for Small Molecules. You will lead impurity risk assessments and shape robust, pragmatic control strategies across the entire product lifecycle, in line with ICH Q3D, ICH Q3C and ICH Q9. This position offers a high level of...Empfohlen
- ...Management interner und externer Kundenbeziehungen Arxada bietet erstklassige Lösungen in zwei klar abgegrenzten Bereichen: Microbial Control Solutions (MCS) konzentriert sich auf Bedrohungen durch Mikroorganismen für Mensch und Umwelt. Dieser Bereich umfasst fünf...EmpfohlenStellvertretung
- ...methodologies Quality Systems & Engineering Support Support quality system activities including: document management change control deviation and non-conformance handling CAPA management Assist the engineering team in establishing: validation...EmpfohlenVollzeit
- ...at the Visp site Act as a key interface between Production, QA, Monitoring, Engineering and EHS in the field of contamination control Plan, lead and execute hygiene-related projects (material transfer, gowning, cleaning, disinfection, cleanroom behavior) Take...Empfohlen
- ...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). Support Engineering on validation, re-qualification and...EmpfohlenVollzeit
- ...administration experience (SAP HANA, Oracle, or SQL Server) ~ Strong understanding of SAP security concepts and role-based access control ~ Experience with monitoring tools such as SAP Solution Manager, EarlyWatch Alerts, and system monitoring utilities ~ Excellent...EmpfohlenRemote job
- ...just a collection of binders, but a living, breathing engine of excellence. System Ownership: Take the wheel on Deviations, Change Control, Document Management, and Training. Risk Mastery: Lead Quality Risk Management (QRM) in line with ICH Q9. You’ll maintain the...Empfohlen
- ...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 (Engineering, Production, QA, EHS) and help shape requalification...Empfohlen