Global Process Quality Specialist — GMP & CAPA

Grifols, S.A; Parets del Vallès; Híbrido; EUR 45.000 - 65.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Occasionally remote

Descripción de la vacante

Grifols, S.A is seeking a Manufacturing Process Evaluation Specialist within the Product Quality area of the Quality Assurance division to support robust process control and compliant documentation.

You will analyze incidents, coordinate corrective actions, review qualification/validation documentation, and prepare audit-ready reports for national and international bodies.

A Health Sciences degree with GMP knowledge and advanced English is required, with at least two years in quality roles.

Formación

• Minimum education in Health Sciences (Pharmacy, Biology, Chemistry); Master or postgraduate in pharma is a plus.
• Knowledge of GMP (Good Manufacturing Practice).
• Knowledge of Basic Statistics.
• Advanced level of English.

Responsabilidades

• Control and document incidents arising in production and control processes.
• Supervise follow-up of corrective or preventive actions from incidents.
• Analyze data and trends from processes.
• Prepare system review reports based on collected/analyzed data.
• Coordinate follow-up groups to communicate process evaluations and trends.
• Review documentation describing production operations and equipment/facilities.
• Review qualification and validation protocols and reports.
• Prepare and deliver documentation requested during audits/inspections by national and international bodies.

Conocimientos

GMP knowledge

Basic statistics

MS Office

SAP

Advanced English

Educación

Health Sciences Degree (Pharmacy, Biology, Chemistry)

Master or Postgraduate degree in pharmaceutical sector

Descripción del empleo

Grifols, S.A is seeking a Manufacturing Process Evaluation Specialist within the Product Quality area of the Quality Assurance division to support robust process control and compliant documentation.

You will analyze incidents, coordinate corrective actions, review qualification/validation documentation, and prepare audit-ready reports for national and international bodies.

A Health Sciences degree with GMP knowledge and advanced English is required, with at least two years in quality roles.