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Quality Assurance Specialist – Audits

Trabajo disponible en: 08001, Barcelona, Cataluna, España
Empresa: Tamarind Intelligence
Tiempo completo puesto
Publicado en 2026-08-10
Especializaciones laborales:
  • Control de Calidad
    Analista de cumplimiento
Rango Salarial o Referencia de la Industria: 42000 - 58000 EUR Anual EUR 42000.00 58000.00 YEAR
Descripción del trabajo

GMP Quality Assurance Technician

Barcelona | Hybrid

About Rephine

Rephine is a global provider of Quality Assurance and GxP Compliance services for the Pharmaceutical, Biotechnology and Medical Device industries.

With offices in Spain, the United Kingdom, India and China, we support leading Life Sciences companies worldwide in maintaining the highest quality and regulatory standards.

We are looking for a GMP Quality Assurance Technician to join our Barcelona team. This is an exciting opportunity for a quality professional who enjoys working in an international environment, managing multiple projects and collaborating with clients and expert auditors across the globe.

The Role

As a GMP Quality Assurance Technician, you will support the planning, coordination and technical review of GMP audits, ensuring compliance with regulatory requirements throughout the audit lifecycle.

Key Responsibilities
  • Coordinate and monitor GMP audit activities from planning through completion.
  • Prepare audit documentation and support the execution of GMP audits.
  • Review audit reports to ensure technical accuracy and regulatory compliance.
  • Request, review and assess Corrective and Preventive Action (CAPA) plans.
  • Provide technical support to clients and internal auditors while maintaining strict confidentiality.
  • Ensure compliance with Rephine's Quality Management System and support internal quality investigations when required.
  • Participate in and, where appropriate, conduct GMP audits.
About You
  • Degree in Pharmacy, Chemistry, Biology, Engineering or another relevant scientific discipline.
  • Minimum two years' GMP experience within the Pharmaceutical, Biotechnology or Medical Device industries.
  • Strong knowledge of FDA, EMA and ICH regulations.
  • Excellent communication and organisational skills.
  • Fluent in English and Spanish; additional languages are an advantage.
  • Able to manage multiple priorities and work independently.
  • Willingness to travel internationally (approximately 20%).
What We Offer
  • Competitive salary, annual bonus and attractive benefits package.
  • Hybrid working model with flexible working arrangements and shorter Fridays.
  • Continuous professional development, including technical and language training.
  • An international, collaborative environment with excellent career development opportunities.
  • Regular team events and a supportive company culture.

If you're looking to build your career with a global leader in Life Sciences Quality Assurance, we'd love to hear from you.

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