QA Manager (m/w/d) freiberuflich für ein Projekt Basel Stadt Startdatum: sofort Referenznummer: /1 Diesen Job teilen oder drucken Aufgaben Verantwortung für klassische Quality Assurance Tätigkeiten im GMP-regulierten Umfeld Bearbeitung und Bewertung von Abweichungen (Deviations), Change Controls und CAPAs
Pierre Fabre Pharmaceuticals Inc. in Basel sucht einen erfahrenen Quality Assurance Officer, der die Implementierung und Pflege von Qualitätsmanagementsystemen im GxP-regulierten Umfeld übernimmt. Sie unterstützen die Sicherstellung der Produktqualität und verbessern kontinuierlich die Prozesse. Der ideale
Wir sind ein junges, dynamisches Consulting-Unternehmen mit Fokus auf die Life-Science-Industrie und arbeiten täglich an hochwertigen, praxisnahen Lösungen für unsere Kundinnen und Kunden. Wir bieten fundiertes Engineering-Quality-Know-how für die Implementierung oder Verbesserung des gesamten technischen Qualitätskonzepts
We are looking for an experienced quality professional to join the IMP Quality Distribution team. In this role, you will help ensure the quality and compliance of Investigational Medicinal Products throughout the global clinical supply chain,
We are looking for an experienced quality professional to join the IMP Quality Distribution team. In this role, you will help ensure the quality and compliance of Investigational Medicinal Products throughout the global clinical supply chain,
Global Quality Assurance Manager m/f/d, Basel-Stadt Job Profil (SI7G04) Life Sciences - Quality Management Basel-Stadt Contracting Vollzeit As soon as possible - 1 year after start date Quality Assurance, GxP, Compliance We are seeking a highly motivated
Gi Life Sciences Basel is seeking a qualified Global Quality Manager (m/f/d) for a leading pharmaceutical company in Basel. The successful candidate will be responsible for global QA oversight of the IMP distribution network and ensure compliance with
We are supporting an international Pharmaceutical company in the search for an experienced MSAT Manager to lead client-facing technical projects and support new product introductions within a GMP aseptic manufacturing environment. Key Responsibilities Act as technical lead
Responsibilities Work in accordance with applicable procedure as per AMAC DOE, POE, MOE, CAME and other AMAC Specification Ensure adequate communication and liaison AMAC internally and especially within the Quality Assurance Team, Maintenance and the Production
Turning change into clear, compelling communication. Proclinical is seeking a Communication and Change Coordinator to support the execution of communication and change initiatives within a fast‑paced transformation environment. This role involves developing communication materials, coordinating stakeholders,