Pharma QA Officer (Temp) - EU GMP & Compliance

Accord Healthcare

Barcelona

Presencial

EUR 32.000 - 46.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

Accord Healthcare in Barcelona is seeking a Quality Assurance Officer for a temporary role to ensure compliant QA practices for EU distribution. You will support the Spanish affiliate in maintaining QA processes and liaise with external partners and internal teams.

Responsibilities include managing the QA system, handling change controls, deviations, CAPA, and product recalls, while overseeing batch documentation and annual quality review.

Formación

  • At least 2 years’ experience in the Quality Assurance department of a pharmaceutical company.
  • Knowledge of QA principles, GMP/GDP requirements in the EEA.
  • Knowledge of Spanish and European QA regulations.
  • Experience in an international work environment.

Responsabilidades

  • Manage and maintain an effective and compliant Quality Management System for Accord Healthcare SLU.
  • Assist in QA policies and procedures.
  • Handle local Change Control, Deviations and CAPA processes.
  • Handle product market returns and liaise with wholesalers and distributors.
  • Review and track Annual Product Quality Review.
  • Collect and analyze quality data and support Management Review Process.
  • Prepare batch documentation for Responsible Person batch release.
  • Handle customer complaints and lead local investigations and CAPAs.
  • Provide support to Marketing, Sales and Customer Service.

Conocimientos

Problem Solving
Drive for Results
Time Management
Peer Relationships

Descripción del empleo

Accord Healthcare in Barcelona is seeking a Quality Assurance Officer for a temporary role to ensure compliant QA practices for EU distribution. You will support the Spanish affiliate in maintaining QA processes and liaise with external partners and internal teams.

Responsibilities include managing the QA system, handling change controls, deviations, CAPA, and product recalls, while overseeing batch documentation and annual quality review.

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