19.09.24 | 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 AGEngineer in science (chemistry, biology) or at least 1 year of experience in a GMP environment - Good knowledge of visual management - Knowledge of BPF - Have a collaborative mindset with the appropriate level of customer service - Autonomous and reliable, highly motivated - Be oriented to meet customer
Später ansehen23.08.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGTo support thechnology transfers activities according to timelines agreed for during the project. - Master or Eng in biology, chemistry, biotechnology or equivalent pharmaceutical experience - Knowledge of GMP - Experience in project Management (PMP, PMI, IPMA) and lab activities - Knowledge in analytical
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
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