Aseptic Purification Technician (GMP)

Grifols; Dún Laoghaire-Rathdown; A distancia; EUR 42.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary package

Group pension scheme with company-mact

Private medical insurance

Descripción de la vacante

Grifols is seeking a Manufacturing Process Technician to support aseptic production and purification in a GMP environment in Ireland. You will operate, monitor, and troubleshoot purification processes, ensuring adherence to cGMP, quality and safety standards while maintaining data integrity and instrument readiness.

You will perform CIP/SIP cleaning, prepare buffers, and execute ultrafiltration, diafiltration and pasteurisation activities to support production schedules.

Formación

• Degree preferred in a scientific discipline and equivalent experience considered.
• Candidates should have 2+ years of experience in a pharmaceutical, GMP-regulated, or other highly regulated manufacturing environment.

Responsabilidades

• Operate, monitor, and troubleshoot purification processes within a GMP-regulated aseptic environment.
• Follow all procedures, policies, quality, health & safety, and regulatory requirements.
• Perform Cleaning-in-Place (CIP) and Sterilisation-in-Place (SIP) and manual cleaning per procedures.
• Set up, operate, and test filtration systems and processes.
• Prepare process buffers and solutions according to batch docs.
• Execute process formulation, ultrafiltration, diafiltration, and pasteurisation tasks.
• Operate large-scale purification and manufacturing equipment per SOPs.
• Own setup and troubleshooting of processing equipment for plasma-derived products.
• Monitor automated SCADA and Windows-based process control systems.

Conocimientos

cGMP knowledge

Attention to detail

Interpersonal skills

Prioritisation

Educación

Degree in scientific discipline

Descripción del empleo

Grifols is seeking a Manufacturing Process Technician to support aseptic production and purification in a GMP environment in Ireland. You will operate, monitor, and troubleshoot purification processes, ensuring adherence to cGMP, quality and safety standards while maintaining data integrity and instrument readiness.

You will perform CIP/SIP cleaning, prepare buffers, and execute ultrafiltration, diafiltration and pasteurisation activities to support production schedules.