ppJob Title: CMO QA Manager /p pSi assicuri di inviare la sua candidatura con tutte le informazioni richieste, come indicato nella panoramica del lavoro riportata di seguito. /p pJob Type: Full time permanent /p pRole Location: Madrid, Spain or Milan, Italy – Hybrid /p pRemuneration: Competitive salary and benefits /p pCpl 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. /p pWorking 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. /p ulliLead and support GMP audits across contract manufacturers, suppliers, and service providers. /li liOversee quality systems activities including deviations, CAPAs, change controls, and investigations. /li liReview and approve critical investigations, ensuring robust root cause analysis and sustainable CAPA implementation. /li liSupport regulatory inspection readiness and interactions with agencies including FDA, EMA, and MHRA. /li liProvide quality leadership for technology transfers, process validation, PPQ, and new product introductions.



/li liLead supplier qualification and ongoing quality performance management activities. /li liMonitor quality metrics and compliance trends to identify and address emerging risks. /li liSupport quality governance forums and collaborate with cross-functional stakeholders to drive continuous improvement initiatives. /li /ul ulliSignificant experience within pharmaceutical quality assurance and GMP-regulated manufacturing environments. /li liProven experience supporting external manufacturing operations, supplier quality, or CMO oversight activities. /li liStrong understanding of GMP requirements, quality systems, investigations, CAPAs, and risk management methodologies. /li liExperience supporting regulatory inspections and audit programmes. /li liExperience within sterile manufacturing, aseptic processing, biologics, or Annex 1 environments. /li liExpertise in sterility assurance, contamination control strategies (CCS), and data integrity. /li liExperience supporting technology transfers, product launches, validation, and complex supply chains. /li /ul pOpportunity to join a growing global pharmaceutical organisation. /p pInternational scope with opportunities to influence quality strategy and culture. /p pHybrid working arrangement based in either Madrid or Milan . /p pInternational travel opportunities as part of a global quality leadership function. xysqume /p pPer questa posizione sono disponibili opzioni di lavoro a distanza/a casa. /p /p #J-18808-Ljbffr

📌 Qa Lead (Hybrid) (Bardi)
🏢 Cpl Life Sciences
📍 Bardi