GxP QA Specialist: Drive Compliance & Quality

Recordati

Zaragoza

Presencial

EUR 40.000 - 65.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

Recordati in Zaragoza, Spain, seeks a Quality professional to maintain the site's Quality System and support regulatory and GxP compliance for pharmaceuticals, medical devices, foods and cosmetics.

The role covers documentation management, CAPAs, change control, training and inspections support, with collaboration across the QA team to ensure batch release readiness and postproduction activities, while upholding our commitment to patient safety.

Formación

  • Requires 2+ years of experience in quality within a health/pharma company.
  • Knowledge of SAP, Veeva or ESKO is valued.

Responsabilidades

  • Maintain the site's Quality System in line with regulatory and GxP standards.
  • Manage the site's Quality Systems Documentation and reviews.
  • Oversee Quality System Management including Non‑Conformances, CAPAs, Change Control, Training and risk analysis.
  • Support Authorities and Client inspections and Auto-inspections.
  • Review batch documentation and coordinate release proposals with the Qualified Person.
  • Review technical documentation of CMOs and GDPs prior to market release.
  • Participate in facilities and equipment qualifications and process validations.
  • Collaborate on quality postproduction tasks (complaints, enquiries, technical info for clients).
  • Perform other functions and projects as needed by Quality Assurance.

Conocimientos

Quality experience
SAP
Veeva
ESKO

Educación

Bachelor's degree in Pharmacy, Science, Engineering

Herramientas

SAP
Veeva
ESKO

Descripción del empleo

Recordati in Zaragoza, Spain, seeks a Quality professional to maintain the site's Quality System and support regulatory and GxP compliance for pharmaceuticals, medical devices, foods and cosmetics.

The role covers documentation management, CAPAs, change control, training and inspections support, with collaboration across the QA team to ensure batch release readiness and postproduction activities, while upholding our commitment to patient safety.

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