Lead CQV Engineer / Lead Validation Engineer

Hiring: Lead CQV Engineer / Lead Validation Engineer Location: Devens, MA (Fully Onsite) Shift: 2nd Shift (2 PM – 10 PM EST) + Weekends Type: W2 contract Pharma/Biotech Environment We are looking for an experienced Lead CQV/Validation Engineer with strong hands-on commissioning, qualification, and validation expertise in regulated pharma/biotech manufacturing environments. Key Skills: • 8+ years of CQV/Validation experience • IQ/OQ execution and operational verification • Process equipment validation: o Bioreactors o Filtration o Chromatography o UF systems • GMP/GDP compliance • Drawing walkdowns & equipment verification • MOC and weld verification • Temperature mapping validation (Ellab preferred) • SIP/CIP cycle development support • Deviation management & audit-ready documentation • eVal experience required (ValGenesis is a plus). Preferred Background: • STEM / Biomedical / Chemical Engineering degree • Prior experience leading validation teams or shift execution activities.