GMP‑Driven QA Technician for Pharmaceuticals

Centrient Pharmaceuticals Netherlands; Santa Perpètua de Mogoda; Presencial; EUR 28.000 - 42.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Local contract

Growth opportunities

Open atmosphere

Descripción de la vacante

Centrient Pharmaceuticals is seeking a Quality Assurance Technician to join our team in Spain. The role focuses on QA activities, audit procedures, and QC processes within a GMP environment.

The ideal candidate holds a Bachelor's degree, speaks English and Spanish fluently, and has at least two years of relevant experience. The position offers a local contract and opportunities for growth in a global pharma setting.

Formación

• Fluent in English and Spanish.
• Knowledge of audit quality procedures.
• Knowledge of Quality Control (QC).
• Minimum of 2 years of experience in a similar role.

Responsabilidades

• Review and sign the Certificate of Analysis for Customers, checking CSO when applicable.
• Review and test preparation shipments.
• Manage internal quality audits and Good housekeeping and propose improvements actions to achieve quality standards.
• Prepare reports which reflect relevant issues related to quality of manufactured products.
• Coordinate Validation plans and Revalidation.
• Supervise the implementation of stability studies.

Conocimientos

Bilingual English and Spanish

Quality Assurance

Audit procedures

Quality Control (QC)

GMP knowledge

Educación

Bachelor's degree

Herramientas

SAP

Descripción del empleo

Centrient Pharmaceuticals is seeking a Quality Assurance Technician to join our team in Spain. The role focuses on QA activities, audit procedures, and QC processes within a GMP environment.

The ideal candidate holds a Bachelor's degree, speaks English and Spanish fluently, and has at least two years of relevant experience. The position offers a local contract and opportunities for growth in a global pharma setting.