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Validation technician – pharma manufacturing

Teruel (44003)
Oxford Global Resources
Publicada el 12 marzo
Descripción

Validation Technician – Pharma Manufacturing

Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud.

Location: Near Zaragoza, Spain

Project Duration: 1 year (possibility of extension)

About the Role:

We are looking for a Validation Technician with hands-on experience in pharmaceutical manufacturing to support process validation, equipment qualification, and batch start-up activities. This role contributes to controlled and efficient commissioning of new production lines.

Key Responsibilities:

- Work in rotational shifts according to production schedules (not 24/7; 3 shifts available)
- Execute manufacturing and technical activities related to process validation, equipment qualification, and start-up batches following GMP protocols and approved procedures
- Ensure strict compliance with site procedures, validation plans, and safety requirements
- Perform cleaning, preparation, routine checks, and technical support during validation phases, including microbiological verification of areas and equipment
- Report deviations or anomalies immediately to the Production Supervisor and Qualified Person
- Verify incoming and outgoing raw materials, consumables, and equipment used during validation and start-up
- Collaborate with MS&T, Engineering, and Quality Assurance to align validation execution with technical and regulatory expectations
- Support training and knowledge transfer to operational teams after validation and start-up activities

Ideal Candidate:

- Education: Scientific or technical background (Higher Vocational Training xpzdshu in Laboratory or University Degree in Chemistry)
- Languages: Basic English reading and writing skills
- Experience: Previous experience in pharmaceutical manufacturing environments
- Flexible and proactive, able to work in shifts (full availability not mandatory)

Why Join:

- Hands-on experience in pharma validation and start-up
- Contribute to new production line commissioning
- Opportunity for project continuity beyond 1 year

How to Apply:

Send your CV via LinkedIn

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