16.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 To Continuous Improvement and the Quality Management System (QMS). Requirements - A degree level (or equivalent) qualification in Science or Engineering, with experience in relevant environments being a strong plus (MEMS, Semiconductors, Nano-Optics). - Knowledge of proposal submission processes to public
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 The QA Engineer CSV will ensure that all computerized systems are validated in accordance with regulatory requirements and industry standards, playing a crucial role in maintaining the quality and compliance of our operations. Main Responsibilities - Validation Management Lead and manage the validation
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Contribute to CRO/Vendor selection and qualification process, assess relevant CROs procedures during selection process to establish a pro-active quality approach, guaranteeing compliance with regulatory requirements. 3. Collaborate with the Clinical Trial Manager and other Functional Area Representatives
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 quality, in the hospital buildings, with preferential rates. Contact et envoi de candidature Contact for information on the function Prof. Jean Louis Raisaro - Head of CDS Group - 021 314 52 25. All of our applications are processed electronically. For this reason, we kindly ask you to apply exclusively
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 A proficient software developer and learn to translate product requirements into code and document your work to be compliant with the BMT Product Development Process (PDP) and Quality Management System (QMS). You will develop your communication skills and become proficient at presenting information to the core
Später ansehen25.08.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Vendor selection and qualification process, assess relevant CROs procedures during selection process to establish a pro-active quality approach, guaranteeing compliance with regulatory requirements - Collaborate with the Clinical Trial Manager and other Functional Area Representatives in the Study Team
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