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 #J-18808-Ljbffr

📌 Interim Quality Manager (Cataluña)
🏢 Barrington James Clinical
📍 Cataluña