CQV Engineer

About the job

We are looking for a skilled and experienced CQV Engineer to join one of our key clients in the Netherlands that is currently undergoing rapid expansion. In this role, you will be instrumental in the commissioning, qualification, and validation of critical systems and process engineering equipment, driving continuous improvement and innovation.

Start Date:

ASAP Duration:

12 months Work Arrangement:

Hybrid. Min 3 days on site

Key Responsibilities: Prepare and manage commissioning and qualification documents for new facilities, including critical system PQs. Create and manage detailed qualification documentation, swiftly addressing deviations and implementing CAPAs. Coordinate with internal teams and external providers for smooth project execution. Present qualification documents during audits, ensuring compliance with quality standards.

Key Requirements: +5 years of experience working in the Biopharma Manufacturing sector. Experience with CAPEX projects is a plus. Proven experience in a regulated GMP environment, with a strong focus on commissioning, qualification, and validation of systems. Excellent communication and writing skills in English are a plus. Ability to work independently, handle multiple projects, and collaborate in a fast-paced, team-oriented environment.

Interested?

Apply below or send your CV to

l.piercy@panda-int.com

to discuss further!