We are seeking a senior Quality Manager to lead and strengthen quality systems within a regulated pharmaceutical environment. This role will play a key part in maintaining GMP compliance, driving continuous improvement, and supporting manufacturing and supply operations through quality oversight. Key Responsibilities Manage and continuously improve the Quality Management System (QMS) in line with GMP and applicable regulatory requirements Lead and oversee deviations, CAPAs, change controls, and risk assessments Support internal, supplier, and regulatory audits and inspections, ensuring inspection readiness Review and approve quality documentation including SOPs, batch records, validation protocols, and reports Partner with Manufacturing, QC, Supply Chain, and Engineering to ensure quality is embedded across operations Support training programs and promote a strong quality culture across the site Required Experience & Qualifications ~ Degree in a scientific or technical discipline (or equivalent experience)



~5+ experience in Quality Assurance within a pharmaceutical manufacturing environment ~ Strong working knowledge of GMP and quality systems ~ Hands‑on experience managing investigations, CAPAs, and change management ~ Confident communicator with the ability to influence cross‑functional teams

What We’re Looking For Proactive, detail‑oriented quality professional Comfortable operating in a fast‑paced, regulated environment Strong problem‑solving skills and ability to balance compliance with operational needs Why Join Opportunity to make a meaningful impact on product quality and patient safety Competitive compensation and professional development opportunities Seniority level ~ Mid‑Senior level

Employment type ~ Contract

Job function ~ Quality Assurance

Industries Pharmaceutical Manufacturing Biotechnology Research Medical Equipment Manufacturing

📌 Quality Assurance Supervisor (Barcelona)
🏢 Barrington James
📍 Barcelona