Pubblicato il 17 giugno
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In this Site Quality Head role, you shape and safeguard the quality strategy for a complex Ivrea manufacturing site. You partner with site and global leadership to ensure compliant operations, continuity, and innovative improvements. You drive a strong quality culture while supporting launches and ensuring every product release meets safety and regulatory standards. You will lead a multidisciplinary quality organization and be pivotal in Health Authority engagements. This position offers high-visibility impact and strategic influence.
Retribuzione / Benefits
Lead the site Quality strategy to ensure full cGMP and regulatory compliance with corporate standards
Establish and sustain a governance model and decision-making framework for the site quality organization
Own and manage site quality systems including deviations, investigations, change control, PQ reviews, and documentation lifecycle
Ensure inspection readiness and coordinate Health Authority inspections and follow-ups
Act as Qualified Person (Deputy) overseeing batch certification and release per legal requirements
Drive quality risk management, escalation processes, and timely health authority notifications
Cultivate a strong quality culture through training, self-inspections, and continuous improvement initiatives
Provide leadership input for talent development, succession planning, and launch readiness
Lead and develop quality leaders and teams to sustain performance and regulatory excellence
Responsabilità
Bachelor's degree in xlwpduy a scientific discipline
Minimum five years of experience in pharmaceutical Quality Assurance or Quality Control in a regulated manufacturing environment
Strong knowledge of cGMP and pharmaceutical quality management systems
Proven experience leading quality organizations with people management and performance oversight
Demonstrated experience preparing for, hosting, and responding to Health Authority inspections
Fluent English, written and spoken, in global cross-functional contexts
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