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About the role
Validation Engineer – EMPQ (Facility & Equipment)
Location: Redmond, WA (100% Onsite) Start Date: February 2026 Experience: Minimum 5 years Duration: Contract
Job Description: We are seeking an experienced Validation Engineer with strong EMPQ expertise to support a new facility startup. This role will focus on protocol development, execution, and documentation for facility and equipment qualification activities.
Key Responsibilities:
Develop and execute EMPQ protocols including IQ, OQ, and PQ
Author and review risk assessments related to equipment and systems
Prepare EMPQ Validation Plans and Qualification Protocols (QPs)
Execute qualification activities and document results
Prepare and finalize Qualification Summary Reports
Ensure compliance with GMP and regulatory requirements
Collaborate with Engineering, Quality, and Operations teams
Required Skills & Qualifications:
Minimum 5 years of validation experience in pharma, biotech, or medical devices
Strong hands-on experience with EMPQ
Proficiency in IQ/OQ/PQ protocol writing and execution
Solid understanding of GMP, FDA, and regulatory expectations
Experience supporting new facility startups preferred
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