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Head of Quality Operations (Pharmaceutical Manufacturing

Trabajo disponible en: 08001, Barcelona, Cataluna, España
Empresa: Page Executive
Tiempo completo puesto
Publicado en 2026-08-08
Especializaciones laborales:
  • Control de Calidad
    Ingeniería de Calidad
  • Farmacéutico
    Fabricación farmacéutica, Ingeniería de Calidad
Rango Salarial o Referencia de la Industria: 120000 - 180000 EUR Anual EUR 120000.00 180000.00 YEAR
Descripción del trabajo
Puesto: Head of Quality Operations (Pharmaceutical Manufacturing)
  • Head of Quality Operations (Pharmaceutical Manufacturing)
  • International pharmaceutical company
About Our Client

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

Job Description

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

  • 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
The Successful Applicant
  • 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.
What’s on Offer

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

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