23.05.24 | Vollzeit | Genève | KPMG AGFor external IT audits in relation to financial statement and regulatory audits - Manage IT assurance engagements (ISAE3402, ISAE3000) to provide independent assurance on the control environment of leading IT service providers - Provide advisory and assurance services in the areas of IT risk management
Später ansehen21.05.24 | Vollzeit, Freelancer | Zürich | KPMG AGOn their challenging journey and covers business, sustainability, technical and regulatory aspects. We follow a multidisciplinary approach and collaborate with the KPMG network to serve our clients globally. KPMG is known for providing clear and consistent solutions in the areas of auditing and advisory services
Später ansehen21.05.24 | Vollzeit, Freelancer | Zürich | KPMG AGOn their challenging journey and covers business, sustainability, technical and regulatory aspects. We follow a multidisciplinary approach and collaborate with the KPMG network to serve our clients globally. KPMG is known for providing clear and consistent solutions in the areas of auditing and advisory services
Später ansehen22.05.24 | Vollzeit | Münchenstein | Primeo EnergieFür Verteilnetzbetreiber und Lieferanten, um die regulatorischen Vorgaben zu kennen und umzusetzen • Überwachung und Bearbeitung der Kaufverpflichtungen von erneuerbaren Energien • Aufsicht über die Bearbeitung der Erzeugungs- und Zugangsanschlüsse bei Produktionsanlagen von erneuerbaren Energien (CRAE/CARD-I
Später ansehen23.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalEmployment application is true to the best of my knowledge. Job Description About the role As Product Quality Expert (PQE) you will report directly to the Head of Quality Compliance & Systems and be responsible for compliance/regulatory activities related to biologic products. The PQE is the representative
Später ansehen14.05.24 | Vollzeit | Lana (Evolène), Laàs, Laas, Cr | HOPPE AGEnglisch in Wort und Schrift - Wollen Bereitschaft, Verantwortung zu übernehmen, eigenverantwortliches und engagiertes Arbeiten, Reisebereitschaft, Einhaltung gesetzlicher - regulatorischer Anforderungen und interner Regeln - Richtlinien - Können hohes Verantwortungsbewusstsein, hohe Sozial
Später ansehen24.05.24 | Vollzeit | Winterthur | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen24.05.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen24.05.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen24.05.24 | Vollzeit | Oftringen | Omya Schweiz AGEstablish and maintain strategy to ensure regulatory compliance of new as well as already marketed food additive, pharmaceutical and cosmetic raw materials - Coordinate Regulatory Affairs registrations and product notifications - Prepare regulatory dossiers (e.g. DMF), liaise and follow up
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