Interim Quality Manager

Barrington James; Barcelona; Presencial; EUR 65.000 - 85.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive compensation

Professional development opportunities

Descripción de la vacante

A leading pharmaceutical firm in Barcelona is looking for a Senior Quality Manager to oversee and enhance quality systems in a regulated environment. You will manage the Quality Management System (QMS) to ensure compliance with GMP standards, lead investigations, and foster a culture of continuous improvement. The role demands 5+ years in Quality Assurance and offers competitive compensation alongside professional development opportunities.

Formación

• 5+ years of experience in Quality Assurance within pharmaceutical manufacturing.
• Strong working knowledge of GMP and quality systems.
• Hands-on experience managing investigations, CAPAs, and change management.

Responsabilidades

• Manage and continuously improve the Quality Management System (QMS)
• Lead and oversee deviations, CAPAs, change controls, and risk assessments.
• Support internal, supplier, and regulatory audits to ensure inspection readiness.
• Review and approve quality documentation including SOPs and validation protocols.

Conocimientos

Quality Management System (QMS)

GMP compliance

Quality Assurance

Regulatory audits

Cross-functional influencing

Educación

Degree in a scientific or technical discipline

Descripción del empleo

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