19.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGReporting to the 'Analytical Development & Innovation Lab Manager' in the Global Analytical Development organization, this role represents an opportunity to significantly contribute to the startup of high-tech analytical laboratories in the BDC, by conducting analytical testing, data evaluation
Später ansehen19.09.24 | Vollzeit | Vaud | Randstad Schweiz AGThe analytical CMC sections of regulatory submissions from source documents, ensuring cGMP compliance and data integrity in alignment with the company's quality standards. Collaborate with CROs and CMOs to ensure the analytical life cycle management and secure supply of licensed products, meeting the approved
Später ansehen17.09.24 | Vollzeit | Aubonne | Randstad Schweiz AGTo ensure appropriate documentation and data management using corresponding IT system, including QMS softwares (TrackWise, ManGo), ERP (SAP), Discoverant… - Assure the timely delivery of required documents (plans, protocols and reports…) as defined in the project plan - Ensure that all process support
Später ansehen09.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGIdentify opportunities, build business cases, and promote the deployment of new technology. - Ensure complete adoption of changes in the field in a tactful and diligent manner, monitor effectiveness, and ensure compliance with EHS and cGMP requirements (including management of change controls, corrective
Später ansehen26.08.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGSampling, aliquoting, utility sampling, HVAC, Gases, corrections of working papers, ) - Perform support activities (autoclave and part washer) - Carrying out the documentation related to your function (e.g. writing working instructions) - Supporting compliance activities (batch review, deviations
Später ansehen23.08.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGCommunication with the Technology Transfer Lead, Site project manager, QC Senior Specialist, QC Associate Managers and with other relevant stakholder. - To contribute to the objectives and the roadmap of the department and group - To enable efficient communication and Strong follow up with the QC Experts
Später ansehen07.08.24 | Vollzeit | Aubonne | Randstad Schweiz AGRegulated industries · Comprehensive knowledge of CSV regulations, guidelines, and industry standards (e.g., FDA, EMA, GAMP) · Proficiency in validation methodologies, tools, and techniques (e.g., risk assessment, test script development, defect management) · Strong analytical, problem-solving
Später ansehen15.07.24 | Vollzeit | Aubonne | Randstad Schweiz AGAnalytical data To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA. - Compliance of QC activities QA support for QC activities including new guidelines, new pharmacopeias versions. Support the implementation of all QC projects. To perform Quality
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