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Validation technician – pharma manufacturing

A Coruña (15008)
Oxford Global Resources
Publicada el 7 marzo
Descripción

Validation Technician – Pharma Manufacturing


La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación.

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 in Laboratory xcskxlj 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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