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

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