Requirements: English
Company: SciPro
Region: North Brabant
SciPro are supporting a leading Pharmaceutical company in their search for a CQV Engineer to join them on a project based in the Netherlands.
They are going through the process of installing a new line, so are looking to expand their expertise within the CQV field.
Key Responsibilities:
- Develop and maintain commissioning and qualification documents for new plants, including PQs for critical systems and ongoing SLC support post-implementation.
- Supervise and resolve deviations, manage changes (GEP and GMP), and implement CAPAs effectively.
- Coordinate efforts between internal teams and external service providers and suppliers to ensure seamless project execution.
- Present qualification documents during audits and inspections, showcasing the outstanding standards maintained.
Key Requirements:
- Proven experience in a regulated GMP environment, specifically in commissioning, qualification, and validation of systems like refrigerators, freezers, clean media, and process engineering equipment.
- Demonstrate independent, flexible work habits, with excellent communication skills and a structured, focused approach to tasks.
- Open to new ideas, agile in thinking, and proactive in problem-solving.
This is an English speaking project, so there is no requirement to speak Dutch, although it would be advantageous.
Please apply within or email me at