QCS StaffingValidation 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
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