Descripción de la oferta
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 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
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