25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalIn Neuchâtel (clinical phase III and commercial). Manage/prepare the necessary supportive documentation for regulatory submissions and for major change projects in Neuchâtel facility. Prepare/Review documentation for change controls, audit observations and regulatory agency questions. Support/Write
Später ansehen24.05.24 | Vollzeit | Bern | Galenica AGPower BI Developer (w/m) 80-100%We will fill this position without personnel service providersWhat you can doDevelop, maintain and manage reporting, dashboards and other BI solutions using Power BIUnderstand and translate business needs and requirements into robust and scalable technical
Später ansehen26.05.24 | Vollzeit | Zürich | Dolder Hotel AGüber ein zertifiziertes Management System nach ISO 90012015 sowie ein Umweltmanagementsystem, welches nach den EarthCheck-Unternehmensstandards zertifiziert ist. Die Abteilungen der Corporate Services - Sales & Marketing, Reservierung, Revenue Management, Public Relations, Quality, Engineering, Human Resources
Später ansehen25.05.24 | Vollzeit | Genève | Lombard OdierA career at Lombard Odier means working for a renowned global wealth and asset manager, with a strong focus on sustainable investing. An innovative bank of choice for private and institutional clients, our independently owned Firm is one of the best-capitalised banking groups in the world, managing
Später ansehen23.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOf internal management as well as across functions and business units. Directs organization of 4 to 5 direct reports (Managers) and approximately 70 indirect headcount. Manages overall coaching, training, development and succession plans for the team. C reates an environment that fosters lifelong learning
Später ansehen27.05.24 | Vollzeit | Winterthur | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, tracking - verification of CAPA commitment implementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating
Später ansehen27.05.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, tracking - verification of CAPA commitment implementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating
Später ansehen27.05.24 | Vollzeit | Winterthur | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, tracking - verification of CAPA commitment implementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalDelivery of test results while upholding the highest standards of quality management practices. Additionally, you'll have the opportunity to step into a managerial capacity, providing backup support and contributing to the seamless flow of our quality assurance processes. If you're passionate about
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalInspection Process You will ensure Compliance with Takeda Quality Management System, regulations and standards, manage Compliance Risk Assessments and represnet your department during regulatory inspections. Ensure the oversite of Quality Systems Pocesses. You will lead a permanent Inspection ready status
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