- Au sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M.Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations du départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez point de contact privilégAu sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M.Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations du départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez point de contact privilég
- In this role, you will join our Manufacturing Operational Support (MOS) service.You will be a key member of a team responsible for developing technical solutions, optimizing the Manufacturing platform, and integrating new molecules. You will act as a catalyst and facilitator for organizational and operational initiatives related to efficiency, productivity, reliability (obsolescence, technology watch), compliance, cost and energy considerations. This is anIn this role, you will join our Manufacturing Operational Support (MOS) service.You will be a key member of a team responsible for developing technical solutions, optimizing the Manufacturing platform, and integrating new molecules. You will act as a catalyst and facilitator for organizational and operational initiatives related to efficiency, productivity, reliability (obsolescence, technology watch), compliance, cost and energy considerations. This is an
- An exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation: You elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation planAn exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation: You elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan
- Joining our Manufacturing Department, you will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells.As Support Technician, you will take part in this exciting adventure by supporting the Manufacturing Shared Services in our development and clinical suites.Your role: Support Operational Activities:Be the expert in the processes under our responsibility (rJoining our Manufacturing Department, you will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells.As Support Technician, you will take part in this exciting adventure by supporting the Manufacturing Shared Services in our development and clinical suites.Your role: Support Operational Activities:Be the expert in the processes under our responsibility (r
