Quality Director - Pharma Manufacturing (Car Allowance)

NMS Recruit Ltd t/a Russell Taylor Group; Oxford; Presencial; GBP 150.000 - 190.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Car allowance

Bonus

Descripción de la vacante

Quality Director role at a major pharmaceutical manufacturing site in Oxfordshire. You will provide strategic direction on quality, compliance and regulatory matters, guiding QA, QP activities and broader Quality Operations.

The role requires leading a sizeable quality function, sustaining GMP compliance, and partnering with senior leadership to drive continuous improvement and strong regulatory relationships.

Formación

• Significant leadership experience in pharmaceutical quality within GMP manufacturing.
• Proven ability to lead large teams including QA and regulatory professionals.
• Strong knowledge of quality systems, batch disposition and regulatory compliance.

Responsabilidades

• Provide overall leadership for the site QA function, incl. QA, QP activities and customer-facing quality.
• Lead and develop a sizeable quality team of managers and specialists.
• Maintain robust quality systems and ensure GMP compliance across operations.
• Oversee deviations, investigations, CAPAs, change control, complaints and risk management.
• Lead regulatory inspections and manage relationships with MHRA, FDA, EMA and authorities.
• Collaborate with Manufacturing to support business priorities while maintaining quality.
• Drive continuous improvement in right-first-time, investigations, and release processes.
• Foster a strong quality culture and succession planning across the organisation.

Conocimientos

Quality leadership

Regulatory compliance

Strategic thinking

People leadership

Educación

Degree in Chemistry/Pharmacy/Biology

Descripción del empleo

Quality Director role at a major pharmaceutical manufacturing site in Oxfordshire. You will provide strategic direction on quality, compliance and regulatory matters, guiding QA, QP activities and broader Quality Operations.

The role requires leading a sizeable quality function, sustaining GMP compliance, and partnering with senior leadership to drive continuous improvement and strong regulatory relationships.