CMO QA Manager

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/799bfk

Di seguito, troverà un'analisi completa di tutti i requisiti per i potenziali candidati e le istruzioni su come candidarsi. CMO QA Manager brFull time permanent brMadrid, Spain or Milan, Italy – Hybrid brCompetitive salary and benefits brCpl 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. brWorking 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. brLead and support GMP audits across contract manufacturers, suppliers, and service providers. brOversee quality systems activities including deviations, CAPAs, change controls, and investigations. brReview and approve critical investigations, ensuring robust root cause analysis and sustainable CAPA implementation. brSupport regulatory inspection readiness and interactions with agencies including FDA, EMA, and MHRA. brProvide quality leadership for technology transfers, process validation, PPQ, and new product introductions.



brLead supplier qualification and ongoing quality performance management activities. brMonitor quality metrics and compliance trends to identify and address emerging risks. brSupport quality governance forums and collaborate with cross-functional stakeholders to drive continuous improvement initiatives. brSignificant experience within pharmaceutical quality assurance and GMP-regulated manufacturing environments. brProven experience supporting external manufacturing operations, supplier quality, or CMO oversight activities. brStrong understanding of GMP requirements, quality systems, investigations, CAPAs, and risk management methodologies. brExperience supporting regulatory inspections and audit programmes. brExperience within sterile manufacturing, aseptic processing, biologics, or Annex 1 environments. brExpertise in sterility assurance, contamination control strategies (CCS), and data integrity. brExperience supporting technology transfers, product launches, validation, and complex supply chains. brOpportunity to join a growing global pharmaceutical organisation. brInternational scope with opportunities to influence quality strategy and culture. brHybrid working arrangement based in either brInternational travel opportunities as part of a global quality leadership function.

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/799bfk