Quality Director

DIATER; Galapagar; Presencial; EUR 80.000 - 120.000; Jornada completa

Descripción de la vacante

A leading company in the allergy diagnostics field is seeking a Quality Director to oversee quality assurance and control activities. This strategic leadership role requires extensive experience in GMP compliance, team management, and regulatory interactions, ensuring high-quality standards in operations and product delivery.

Servicios

Competitive compensation and benefits package

Collaborative and supportive working environment

International working environment

Formación

• At least 10 years of leadership experience in QA and QC.
• Minimum 10 years of QP experience in pharmaceuticals.
• Deep knowledge of GMP standards and regulatory requirements for biologics.

Responsabilidades

• Lead and manage all QA and QC activities, ensuring compliance and continuous improvement.
• Oversee product release processes and inspection readiness.
• Collaborate with cross-functional teams to embed quality across product lifecycle.

Conocimientos

Leadership

Strategic Thinking

Problem Solving

Compliance

Communication

Educación

University degree in Pharmacy

Advanced degree

Descripción del empleo

Our company is a well-established specialist in the field of allergy diagnostics and treatments, offering an extensive portfolio of high-quality products designed to improve the quality of life for patients suffering from allergic diseases. With decades of experience and a strong reputation for scientific excellence, patient focus, and regulatory compliance, we are committed to supporting healthcare professionals and patients with trusted and innovative solutions.

Position Summary

We are seeking an experienced and committed Quality Director to lead and oversee all Quality Assurance (QA), Quality Control (QC) activities, with strategic accountability for maintaining GMP compliance across manufacturing and laboratory operations. This role will also directly manage the Qualified Person (QP) team to ensure seamless batch release processes while driving continuous improvement of lifecycle management. Reporting directly to the General Manager, you will ensure our operations continue to meet the highest standards of quality, compliance, and safety — supporting the delivery of products that meet both patient needs and regulatory expectations. This is a strategic leadership role, responsible for driving a quality-centric culture, ensuring compliance with applicable regulations, and maintaining robust quality systems in a regulated environment.

Key Responsibilities

• Act as principal qualified person, leading the team of deputy qualified persons.
• Provide strategic and operational leadership to the Quality Assurance and Quality Control teams, ensuring alignment with company objectives and regulatory requirements.
• Ensure full compliance with applicable national and international standards, including EMA, FDA, NMPA, and other relevant pharmaceutical authorities and regulatory frameworks.
• Lead, manage, and continuously improve the Quality Management System (QMS) to ensure its effectiveness in supporting quality compliance, company quality policy, product quality, and production sustainability.
• Oversee product release processes, laboratory operations, deviation investigations, change control, CAPA, and supplier qualification programs.
• Act as the primary point of contact for regulatory inspections, customer audits, and certification bodies, representing the quality organization with confidence and credibility.
• Monitor and report quality performance through KPIs and dashboards, ensuring proactive identification and mitigation of risks.
• Collaborate cross-functionally with Manufacturing, R&D, Regulatory Affairs, and Commercial teams to embed quality across the product lifecycle.
• Lead and mentor the quality organization to strengthen technical expertise, foster continuous improvement, and maintain a strong culture of compliance and accountability.
• Contribute to company-wide initiatives in digital transformation, operational excellence, and innovation from a quality perspective.

Candidate Profile

• University degree in Pharmacy; an advanced degree is a plus.
• Minimum 10 years of progressive leadership experience in Quality Assurance and Quality Control, ideally within the allergy/immunotherapy sectors, biotech, or pharmaceutical.
• Minimum 10 years of QP experience in pharmaceuticals.
• Deep knowledge of NPP, GMP standards, and regulatory requirements applicable to biologics and allergy-related products.
• Successful experience leading teams through regulatory inspections and third-party audits.
• Strong strategic thinking with hands-on leadership and problem-solving skills.
• Excellent communication skills in both Spanish and English.
• High integrity, attention to detail, and a commitment to patient safety and product excellence.
• Good relationships with authorities, especially with AEMPS.

What We Offer

• A key leadership role within a respected, patient-centered organization.
• The opportunity to shape quality strategies and impact the health and wellbeing of allergy patients.
• A collaborative and supportive working environment.
• Competitive compensation and benefits package.
• International working environment.