LAVORO HEAD OF QUALITY ASSURANCE PARMA, EMILIA ROMAGNA

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... therefore, we strive to continuously...

Experience required at least 6-8 years of experience in quality assurance in the pharmaceutical industry... knowledge of total quality management standards and principles...

Good knowledge of the analytical characterization of inhalation devices... study monitor of stability studies... support to the critical quality attribute identification...

Main responsibilities in coordination with the head of scenario planning and insight & digital solutions unit ensures the effective development and management...

Integration of different systems... be responsible for the qualification of spreadsheets used in gpv... psmf), principles of computer system validation (csv), technical...

Good knowledge of the quality documentation management... knowledge of gxp regulations and quality standards... main responsibilities the person will: support the...

Knowledge of gmp/cgmp regulations... good knowledge of incoterms regulations... good understanding of pharmaceutical industry processes... execute distribution activities...

Respect the code of conduct, policy anti-bribery and other policies of our program of ethics and integrity...   manage and follow-up of industrial purchase orders...

Interviews with the auditees, issue log implementation)  –    support the test of execution phase of the audits (e... we believe that the success of chiesi is built...

Planning and managing of the internal tax audits... reviewing, approval and submission of all fiscal returns (e... we believe that the success of chiesi is built...

To guarantee quality of statistical output produced by external provider, to program tools to support data review activities and data visualization, to collaborate...

Ensure project deliverables adhere to regulatory guidelines and quality standards... experience required minimum of 7 years experience in regulatory affairs...