22 set - Livorno
Chiesi
Overview 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.
Retribuzione / Benefits relocation support flexible working arrangements remote work options Monitor and analyze quality data, identify trends, and drive improvement actions Prepare periodic QMS performance reports for management Govern and promote a culture of quality and continuous improvement across the site Degree in scientific subjects (Chemistry, Pharmaceutical Chemistry and Technology, Engineering) At least 5 years of pharmaceutical/biopharmaceutical experience in QA, Production, and Process Technology Specialized expertise in GMP compliance improvement processes Fluent English (written and spoken) Strong teamwork and cross-functional collaboration Quality data analysis and trend identification Root cause analysis and CAPA implementation
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