Analyst Jobs in Visp
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Suchergebnisse - Analyst Jobs in Visp
Gi Life Sciences BaselVisp
Für ein führendes Pharmaunternehmen suchen wir für einen temporären Einsatz eine/n qualifizierte/n
QC Analyst Mikrobiologie (m/w/d)
QC Analyst für Mikrobiologie (m/w/d)
Allgemeine Informationen:
Arbeitsplatz: Visp
Startdatum: Geplante Dauer der...
LonzaVisp
Chemie – wir meistern die ganze Bandbreite.
Was macht diese Rolle so spannend?
Als Analyst in unserem QC 24/7 Analytical Services Team haben Sie die Wahl: Entweder spezialisieren Sie sich auf eine der hochmodernen Technologien oder Sie erweitern Ihr Know...
Gi Life Sciences BaselVisp
QC Analyst für Mikrobiologie (m/w/d)
Allgemeine Informationen:
Arbeitsplatz: Visp
Startdatum:
Geplante Dauer der Anstellung: bis
Workload: 100%
Ihre Aufgaben
• Durchführung mikrobiologischer Routineanalysen sowie Auswertung, Review und...
RealVisp
System (QMS) initiatives. The role focuses on data migration, data analysis, and the deployment of the Veeva Vault system at the local site. This position is ideal for candidates with experience in GMP‑regulated environments and strong technical affinity...
ManpowerVispjobcourier.ch
Manpower
For one of our pharma clients based in Visp, we are looking for a Data Analyst to cover a contract role from 04/05/2026 to 03/10/2026.
Description:
Key Responsibilities
• Supporting data migration and data analysis activities related...
ProclinicalVisp
Drive digital quality forward by transforming critical QMS data into a streamlined, future‑ready Veeva Vault system.
Proclinical is seeking a Data Analyst to support data migration and analysis activities related to Quality Management System (QMS)...
Gi Group SA SwitzerlandVisp
Qualité Biochimie, vous contribuez à la garantie de la qualité des produits en réalisant des analyses biochimiques dans le respect des BPF et des règles de sécurité.Vos compétences :· d analyses de routine en biochimie, en particulier ELISA.· à la mise en...
Coopers Group AGVisp
and facilities:
• Validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
• The validation documentation deliverables include URS...
Coopers Group AGVisp
and facilities:Validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.The validation documentation deliverables include URS, DQ, FMEA, Risk...
Randstad (Schweiz) AGVisp
Conduct
thorough and well-documented investigations of deviations in the
manufacturing process of monoclonal antibody-based
products.
• Perform root cause
analyses using structured methodologies (e.g., 5-Why, Ishikawa, FMEA).
• Develop, implement...
Coopers Group AGVisp
and facilities:Validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.The validation documentation deliverables include URS, DQ, FMEA, Risk...
Gi Group SA SwitzerlandVisp
de la qualité des produits en réalisant des analyses biochimiques dans le respect des BPF et des règles de sécurité.
Vos compétences :
• Réalisation d'analyses de routine en biochimie, en particulier ELISA.
• Participation à la mise en place...
InGoedeBanen.nlVisp
Conduct thorough and well-documented investigations of deviations in the manufacturing process of monoclonal antibody-based products.
• Perform root cause analyses using structured methodologies (e.g., 5-Why, Ishikawa, FMEA).
• Develop, implement...
Coopers Group AGVisp
and facilities:Validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.The validation documentation deliverables include URS, DQ, FMEA, Risk...
Coopers Group AGVisp
and facilities:Validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.The validation documentation deliverables include URS, DQ, FMEA, Risk...
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