Position Overview
Roles & Responsibilities:
Lead qualification of cleanroom facilities and large-scale manufacturing process equipment, including centrifuges and filter presses
Author, execute, and close validation protocols and final reports with minimal oversight
Conduct construction walks, pre-check P&IDs, and identify, communicate, and escalate field and design issues
Review and approve protocols, SOPs, TOPs, and vendor submittals against specifications and quality standards
Drive execution planning, scheduling, and cross-functional coordination using DeltaV, Kneat, Veeva, Bluebeam, and MS Education & Experience: Bachelor's degree in engineering, Life Sciences, or a related field
+ years of experience in validation within a regulated industry (, pharma, biotech)
Proven experience qualifying cleanroom facilities and manufacturing-scale process equipment
Direct experi...