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

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