Validation Engineer

Our client operates within the Biopharma Domain in the Netherlands. The site is currently undergoing a transformation project from R&D to CMO facility and is in need of additional Validation support to hit timelines.

You will be responsible for supporting the Validation activities on-site for the equipment (including clean utilities); and collaborate on execution and documentation activities. Your focus will be on supporting the team to ensure the site is qualified and validated for GMP compliant for inspections. 

Essential Requirements

• Education Requirement: Degree in Engineering or equivalent.

• At least 4-5 years experience in validation, CQV, or Project Engineering positions within a GMP environment.

• Experience in writing, executing, and reporting qualification protocols, along with reviewing protocols and reports.

• +3 years experience with Equipment Qualifications (IQ/OQ/PQ) and Routine Equipment (Re-)Qualification.

Practicalities

• Start Date: ASAP

• Contract Duration: 6 months (Extension possible)

• Location: Leiden

• Additional: The interview process is fast: A Teams interview with the Director of Engineering and Validation Manager (max 1 hour), followed immediately by a decision. 

Interested?

Interviews and offers can move quickly. Send your CV to c.girdwood@panda-int.com today to secure your spot in the process.