Quality System e Compliance Specialist
Pubblicato il 18-10-2026 - Chiesi in L'Aquila
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