Cmo Qa Manager

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7aa1uk

Di seguito, troverà un'analisi completa di tutti i requisiti per i potenziali candidati e le istruzioni su come candidarsi. CMO QA Manager Scorra verso il basso per una panoramica approfondita di questo lavoro e dei requisiti per i candidati. Invii la sua candidatura facendo clic sul pulsante "Candidati". Tempo pieno permanent Madrid, Spain or Milan, Italy – Hybrid Competitive salary and benefits Cpl Life Sciences is partnering with a leading international pharmaceutical organisation to recruit a CMO QA Manager. This is an exciting opportunity for an experienced quality professional to take ownership of quality oversight activities across a global network of Contract Manufacturing Organisations (CMOs) and external partners. Working within a highly visible international quality function, you will play a key role in ensuring GMP compliance, driving quality excellence, and supporting the delivery of safe, high-quality products to patients worldwide. Lead and support GMP audits across contract manufacturers, suppliers, and service providers. Oversee quality systems activities including deviations, CAPAs, change controls, and investigations. Review and approve critical investigations, ensuring robust root cause analysis and sustainable CAPA implementation. Support regulatory inspection readiness and interactions with agencies including FDA, EMA, and MHRA. Provide quality leadership for technology transfers,



process validation, PPQ, and new product introductions. Lead supplier qualification and ongoing quality performance management activities. Monitor quality metrics and compliance trends to identify and address emerging risks. Support quality governance forums and collaborate with cross-functional stakeholders to drive continuous improvement initiatives. Significant experience within pharmaceutical quality assurance and GMP-regulated manufacturing environments. Proven experience supporting external manufacturing operations, supplier quality, or CMO oversight activities. Strong understanding of GMP requirements, quality systems, investigations, CAPAs, and risk management methodologies. Experience supporting regulatory inspections and audit programmes. Experience within sterile manufacturing, aseptic processing, biologics, or Annex 1 environments. Expertise in sterility assurance, contamination control strategies (CCS), and data integrity. Experience supporting technology transfers, product launches, validation, and complex supply chains. Opportunity to join a growing global pharmaceutical organisation. International scope with opportunities to influence quality strategy and culture. xrdztoy Hybrid working arrangement based in either International travel opportunities as part of a global quality leadership function.

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7aa1uk