Le poste
04Major Accountabilities:
- Plan, coordinate, and support sampling activities, including execution, documentation, and alignment with project and routine laboratory needs.
- Review, evaluate, and approve analytical test results for release, stability, and project-related activities in accordance with applicable procedures.
- Prepare, review, and approve analytical protocols, reports, trend analyses, KPIs/KQIs, and registration-related documentation.
- Lead or contribute to analytical project activities, including method implementation, analytical transfers, new product introduction, and routine laboratory readiness.
- Serve as Single Point of Contact or Subject Matter Expert for assigned products, pipeline activities, external initiatives, audits, inspections, and technical assessments.
- Manage deviations, OOx investigations, CAPA definition, analytical weak points, and continuous improvement actions to ensure robust laboratory performance.
- Contribute to supplier qualification, service provider management, contracts, SLAs, SOWs, QAAs, budgeting activities, and cross-functional governance meetings.
- Ensure all activities comply with cGxP, data integrity, Quality, and HSE requirements, including equipment maintenance, calibration planning, training, risk identification, and safe working practices.
01Plan, coordinate, and support sampling activities, including execution, documentation, and alignment with project and routine laboratory needs.
02Review, evaluate, and approve analytical test results for release, stability, and project-related activities in accordance with applicable procedures.
03Prepare, review, and approve analytical protocols, reports, trend analyses, KPIs/KQIs, and registration-related documentation.
04Lead or contribute to analytical project activities, including method implementation, analytical transfers, new product introduction, and routine laboratory readiness.
05Serve as Single Point of Contact or Subject Matter Expert for assigned products, pipeline activities, external initiatives, audits, inspections, and technical assessments.
06Manage deviations, OOx investigations, CAPA definition, analytical weak points, and continuous improvement actions to ensure robust laboratory performance.
07Contribute to supplier qualification, service provider management, contracts, SLAs, SOWs, QAAs, budgeting activities, and cross-functional governance meetings.
08Ensure all activities comply with cGxP, data integrity, Quality, and HSE requirements, including equipment maintenance, calibration planning, training, risk identification, and safe working practices.
