31.05.24 | Vollzeit | Val-d'Illiez | WuXi AppTecAnd/ or Packaging Operations in monitoring quality and performance metrics and acts as a referee for the operational team for GMP systems, documentation and training. He/she is the manufacturing referee for the batch record creation and revision in PAS-X electronic system. - This is a Long-Term Temporary Position
Später ansehen31.05.24 | Vollzeit | Val-d'Illiez | WuXi AppTecBased on the need quality metrics, release planning, etc. This position will be working closely with the QA Operations team to support day to day activities to ensure lean release of finished/semi-finished product, bulk product, or raw materials for production, as well as to contribute to QA Ops
Später ansehen31.05.24 | Vollzeit | Val-d'Illiez | WuXi AppTecThis position is a key leadership role being responsible for the direct management of individual contributors, supervisors and managers. This position is a role model for the WuXi values and competencies. Job Summary The Associate Director Quality Contro l is charged with Overseeing the Quality
Später ansehen31.05.24 | Vollzeit | Val-d'Illiez | WuXi AppTecQuality Control is responsible to support the entire Couvet site to ensure that each analytical and microbiological testing is performed in compliance with the site’s Quality Management Systems (QMS), the cGMP, the applicable laws, regulations, and standards, and in compliance with the Product’s
Später ansehen01.06.24 | Vollzeit | Nyon | HaleonThe purpose of this role is to provide regulatory management, governance and expertise to one category, sub-category, brand or a portfolio of products such that our products are successfully introduced or maintained Globally. The individual will build a network of collaborative relationships within
Später ansehen01.06.24 | 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 ansehen01.06.24 | Vollzeit | Nyon | HaleonThe future. It’s an opportunity to be part of something special. About the role The purpose of this role is to Serving as the main contact with the Global Quality Organization to ensure timely implementation and correct usage of the Haleon Quality System on site. Acting as the Risk Management Process Owner
Später ansehen01.06.24 | 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 | Basel (Basel-Stadt) | BakerHicksAnd positioning BakerHicks and its Clients in advantageous positions when procuring goods or services in an engineering and construction environment Development and negotiation of terms and conditions in line with the form of contract Comply with BakerHicks’ and Client Quality Assurance and Management system
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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