- As a MOS Compliance Expert at Merck, you will play a pivotal role in the Production department, especially in the Compliance field, by conducting critical and transversal complex investigations, ensuring data integrity, leading Corrective and Preventive Actions (CAPA), maintaining compliance with Good Manufacturing Practices (GMP), and overseeing classified environment monitoring activities. Your responsibilities will also include overseeing project qualitAs a MOS Compliance Expert at Merck, you will play a pivotal role in the Production department, especially in the Compliance field, by conducting critical and transversal complex investigations, ensuring data integrity, leading Corrective and Preventive Actions (CAPA), maintaining compliance with Good Manufacturing Practices (GMP), and overseeing classified environment monitoring activities. Your responsibilities will also include overseeing project qualit
- 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
- Key Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scrKey Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scr
- We are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key RespWe are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key Resp
- 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
- 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
