Validation Engineer (CQV, GMP, Life Sciences)

Validation Engineer (CQV, GMP, Life Sciences) Location: Greater Chicago Salary: $70-100K + Bonus + Benefits No Sponsorship, No Relocation Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer who wants hands‑on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work. What You’ll Do Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols Work on validation of lab systems, equipment, and utilities Partner with engineering, validation teams, and lab stakeholders Assist with project scheduling, coordination, and resource planning Support commissioning & qualification (CQV) activities across projects Contribute to GMP / GxP documentation and compliance efforts Learn to lead validation workstreams and progress into a Validation Project Lead role What We’re Looking For 5+ years of experience in: Validation Engineering CQV (Commissioning, Qualification, Validation) or GMP-regulated environments (Pharma / Biotech) Strong understanding of: GMP / GxP / FDA regulations Validation lifecycle (IQ/OQ/PQ) Ability to work cross-functionally with engineering, QA, and operations teams Strong communication and problem‑solving skills Coachable, driven, and motivated to grow into leadership Requirements Bachelor’s degree in Engineering, Life Sciences, or related field Willingness to travel regionally (project-based work) Experience with validation documentation, protocols, and execution Nice to Have Experience with lab systems, utilities, or manufacturing equipment validation Exposure to commissioning activities (C&Q / CQV) Familiarity with AI tools for validation or documentation Why This Role Hands‑on experience across pharma validation projects Clear path into senior validation or project leadership roles Work alongside experienced engineers in regulated environments #J-18808-Ljbffr