Global Manufacturing Process Quality Specialist

Grifols; Parets del Vallès; Híbrido; EUR 36.000 - 52.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Permanent position

Occasional remote work

Descripción de la vacante

Grifols is seeking a Manufacturing Process Evaluation Specialist within the Product Quality area of the Quality Assurance division. You will control and document incidents in production and control processes, and supervise corrective actions with data-driven insights.

Requirements include Health Sciences degree, GMP knowledge, statistics, MS Office, SAP, advanced English, and at least 2 years in a similar quality role.

Formación

• Health Sciences Degree required; Master/Postgraduate in pharma preferred.
• Knowledge of GMP is required.
• Knowledge of Basic Statistics is required.
• Proficiency in MS Office and SAP.
• Advanced level of English.
• At least 2 years of experience in a similar Quality role.

Responsabilidades

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

Conocimientos

GMP knowledge

Basic Statistics

MS Office

SAP

English (Advanced)

Educación

Health Sciences Degree (Pharmacy, Biology, Chemistry)

Master or Postgraduate in pharmaceutical sector (preferred)

Descripción del empleo

Grifols is seeking a Manufacturing Process Evaluation Specialist within the Product Quality area of the Quality Assurance division. You will control and document incidents in production and control processes, and supervise corrective actions with data-driven insights.

Requirements include Health Sciences degree, GMP knowledge, statistics, MS Office, SAP, advanced English, and at least 2 years in a similar quality role.