02 ott - Bardi
Chiesi
In 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.
comprehensive healthcare programs
work-life balance initiatives
relocation support
flexible working arrangements
remote work options
Develop and implement QMS processes, procedures, and documentation to meet quality standards
Monitor and analyze quality data, identify trends, and drive improvement actions
J-18808-Ljbffr
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