ppIn this role you will lead and optimize the Quality Management System to ensure GMP, FDA and EU compliance across the site.
You will partner with cross-functional teams to drive quality improvements, manage inspections, training, and documentation, and report on QMS performance.
You will enable a culture of quality and continuous improvement, shaping robust processes for materials, manufacturing, and release specifications.
This is a chance to contribute to a globally recognized biopharmaceutical group focused on sustainable health outcomes.
/pullicomprehensive healthcare programs /liliwork-life balance initiatives /lilirelocation support /liliflexible working arrangements /liliremote work options /liliDevelop and implement QMS processes, procedures, and documentation to meet quality standards /liliMonitor and analyze quality data, identify trends, and drive improvement actions /li /ul /p #J-*****-Ljbffr
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