You will define and propose the qualification/validation strategy for the systems and production equipment you are responsible for (routine and/or project activities).You will participate in conducting quality risk assessments.You will define the validation/cleaning Postuler | Plus d'offres Equipment Laboratory Valid. Associat Plus d'offres - Braine-l'Alleud
including utilities and stores.What you'll do:You will take charge of qualification projects for systems and production equipment and/or laboratoryequipment assigned to you,..
etc.).You will coordinate/execute/verify qualification/validation tests.You will inform your hierarchy and stakeholders of any deviations and suggest necessary corrective actions.You will make necessary decisions in case of deviations impacting the qualification strategy.You will en..
You will coordinate Periodic Reviews under your responsibility.You will ensure compliance with the Periodic Review schedule (Compliance Requirement).You will contribute to the establishment of an effective and standardized approach to qualifying systems and production equipment.You ..
Belgium.About the role:You will be responsible for qualification activities of Production and/or Development equipment (including utilities) as well as GMP laboratoryequipment,..
/Knowledge of IT/Computerized System Validation techniques.Knowledge of cGMP,..in accordance with the Validation Master Plan (VMP) of the Braine-l'Alleud Site.You will ensure the validation of manufacturing processes in compliance with cGMP,..
You will ensure the qualified status of production equipment according to the initial qualification and periodic review schedule.You will ensure the permanent auditability (Permanent Inspection readiness) of qualification records for systems and production equipment.Who you'l..
