17.04.24 | Vollzeit | Ascom Schweiz AGAdministration and user support · Supporting users and document owners with training, issue solving and improvements · Monitoring DMS and document status and providing regular communication · Maintaining DMS compliance with updated templates, coordinating change management, and validation Projects and continuous
Später ansehen17.04.24 | Vollzeit | Ascom Schweiz AGAdministration and user support · Supporting users and document owners with training, issue solving and improvements · Monitoring DMS and document status and providing regular communication · Maintaining DMS compliance with updated templates, coordinating change management, and validation Projects and continuous
Später ansehen17.04.24 | Vollzeit | Frankfurt am Main, Mägenwil | Ascom Schweiz AGSystem administration and user support · Supporting users and document owners with training, issue solving and improvements · Monitoring DMS and document status and providing regular communication · Maintaining DMS compliance with updated templates, coordinating change management, and validation Projects
Später ansehen17.04.24 | Vollzeit | Ascom Schweiz AGSystem administration and user support · Supporting users and document owners with training, issue solving and improvements · Monitoring DMS and document status and providing regular communication · Maintaining DMS compliance with updated templates, coordinating change management, and validation Projects
Später ansehen16.04.24 | Vollzeit | Solothurn | Randstad Schweiz AGAs import/export release to Switzerland as per Swiss Regulation (812.212.1) and European Directive 2001/83/EC, 2017/1572 as well as delegated regulation 2017/1569. The RP release delegate is responsible for ensuring that each individual batch has been manufactured in compliance with laws in force
Später ansehen10.04.24 | Vollzeit | Solothurn | Randstad Schweiz AGTheir compliance is key. Solid technical knowledge is mandatory to understand the content, enabling e.g. the review of P&IDs. Tasks & Responsibilities - Share and enforce the applicable standards & practices with the project team and Work Package Owners (= SMEs of the EPCMQ or suppliers) - Proactively align
Später ansehen03.04.24 | Vollzeit | Visp | Randstad Schweiz AGThis, the TPL is in close collaboration with the technical team during the design phase, FATs - SATs and commissioning until IQ - OQ. Sharing technical standards and auditing their compliance is key. Solid technical knowledge is mandatory to understand the content, enabling e.g. the review of P&IDs
Später ansehen28.03.24 | Vollzeit | Lausanne | Randstad Schweiz AGContributing to the development of training materials on compliance topics. - Supporting various Quality Management System activities, including Corrective and Preventive Actions (CAPA), quality plans, and audits. Qualifications - Strong knowledge of EU Medical Device Regulation (EU) 2017/745, European
Später ansehen16.03.24 | Vollzeit | Port, Porţ | RÜSCH AUSTRIA Gesellschaft m.b.H.Responsible for the establishment, execution, maintenance and Global Harmonization of the quality management system (QMS), in compliance with ISO13485, GDPMDS - QMS management and support of the QMS activities including internal, supplier and external audits. - Perform regular internal audits and trainings
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