Validation Engineer

Overview

Validation Engineer - Redmond, Seattle - 4-6 Month Contract
Our client, a global biotechnology organisation, is recruiting for a Validation Engineer to join their capital project in Redmond. This new build facility will house a therapeutic protein production plant, and we are looking for a Validation Engineer to help expand our client's biotech operations throughout Europe. As the Validation Engineer you will be responsible for implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.

• Identify gaps, risks, and improvement opportunities, escalating issues where required.
• Support the maintenance of validated status through impact assessments, requalification planning, and validation updates.
• Maintain validation files and ensure documentation is audit-ready at all times.
• Participate in internal and external audits, providing subject-matter expertise on validation lifecycle and periodic review processes.

• Experience in pharmaceutical, biotech, or other regulated GMP environments.
• Strong understanding of validation principles (IQ/OQ/PQ), equipment qualification, and process validation.
• Familiarity with regulatory guidelines including EU GMP Annex 15, FDA 21 CFR Parts 210/211, and data integrity expectations.
• Excellent analytical and documentation skills with a high attention to detail.

If this role is of interest, please apply now!