Global Manufacturing Process Quality Analyst

Grifols Shared Services North America, Inc; Parets del Vallès; Presencial; EUR 42.000 - 63.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Permanent contract

Descripción de la vacante

Grifols Shared Services North America, Inc is hiring a Manufacturing Process Evaluation Specialist in Parets del Vallès to support quality assurance in manufacturing. You will monitor incidents, lead corrective actions, analyze process data, and prepare review reports for audits and inspections.

The role requires a Health Sciences degree (pharmacy/biology/chemistry), GMP knowledge, statistics, English fluency, and 2+ years in quality. We offer a permanent contract in a global healthcare group.

Formación

• You have a Health Sciences Degree (Pharmacy, Biology, Chemistry) and may hold a Master or postgraduate in pharma.
• You know GMP and basic statistics and are proficient with MS Office and SAP.
• You have advanced English and at least 2 years in a similar quality role.

Responsabilidades

• Control and document incidents in production and control processes.
• Supervise corrective or preventive actions from incidents.
• Analyze data and trends from processes.
• Prepare system review reports from analyzed data.
• Coordinate follow-up groups for communication of evaluations and trends.
• Review production operation documentation and equipment/facilities.
• Review qualification and validation protocols and reports.
• Prepare and deliver audit/inspection documentation.

Conocimientos

GMP knowledge

Basic statistics

Advanced English

QA experience

MS Office

SAP

Educación

Health Sciences Degree

Master or postgraduate in pharmaceutical sector

Herramientas

MS Office

SAP

Descripción del empleo

Grifols Shared Services North America, Inc is hiring a Manufacturing Process Evaluation Specialist in Parets del Vallès to support quality assurance in manufacturing. You will monitor incidents, lead corrective actions, analyze process data, and prepare review reports for audits and inspections.

The role requires a Health Sciences degree (pharmacy/biology/chemistry), GMP knowledge, statistics, English fluency, and 2+ years in quality. We offer a permanent contract in a global healthcare group.