Head of Quality Operations (Pharmaceutical Manufacturing)

Barcelona Ciudad Permanente Ver descripción del puesto
Our client is an international pharmaceutical company undergoing a significant transformation of its Quality organization. As part of this journey, the company is strengthening its leadership team to support operational excellence, quality culture development and regulatory readiness across its manufacturing network.

Added 06/08/2026

  • Head of Quality Operations (Pharmaceutical Manufacturing)
  • International pharmaceutical company

¿Dónde vas a trabajar?

International pharmaceutical company undergoing a significant transformation of its Quality organization.

Descripción

Reporting to the Global Quality Director, the successful candidate will provide strategic and operational leadership across pharmaceutical manufacturing quality activities.

Key responsibilities include:

  • Leading Quality Assurance and Quality Control activities across multiple pharmaceutical manufacturing sites.
  • Ensuring GMP compliance throughout manufacturing, packaging, testing and batch disposition processes.
  • Driving inspection readiness and supporting regulatory inspections and audits.
  • Providing quality oversight for deviations, investigations, CAPAs, change controls and validation activities.
  • Partnering closely with Manufacturing, Supply Chain and Technical Operations leaders to ensure product quality and business continuity.
  • Leading quality culture and continuous improvement initiatives across the organization.
  • Developing and coaching quality leadership teams while building organizational capability.
  • Supporting strategic projects including new product introductions, technology transfers and transformation initiatives

¿A quién buscamos (H/M/D)?

  • Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Engineering or related Life Sciences discipline.
  • Significant experience in Quality leadership roles within pharmaceutical manufacturing environments.
  • Strong understanding of GMP regulations and pharmaceutical quality systems.
  • Proven experience supporting or leading regulatory inspections and audits; FDA inspection exposure is considered a strong advantage.
  • Experience working closely with manufacturing and operations leadership teams.
  • Strong leadership, stakeholder management and influencing skills.
  • Ability to lead large teams within complex and highly regulated environments.
  • Experience driving quality culture and organizational transformation initiatives is highly desirable.



¿Cuáles son tus beneficios?

Great opportunity to join an international pharmaceutical company undergoing a significant transformation of its Quality organization.

Ver más ofertas de empleo
Andrea Sileo
Indicar número de referencia para la oferta
JN-082026-7078566

Resumen de empleo

Sector
Healthcare
Sub Sector
Registros
Industria
Healthcare / Pharmaceutical
Localización
Barcelona Ciudad
Tipo de Contracto
Permanente
Nombre del consultor
Andrea Sileo
Número de referencia
JN-082026-7078566

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