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 (Madrid)
🏢 Barrington James
📍 Madrid