Validation Engineer (CQV, GMP, Life Sciences)

VBB

$70K — $100K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years of experience in Validation Engineering or GMP-regulated environments
  • Strong understanding of GMP/GxP/FDA regulations
  • Ability to collaborate with engineering, QA, and operations teams
  • Excellent communication and problem-solving skills
  • Coachable, driven, and motivated for leadership roles
  • Bachelor's degree in Engineering, Life Sciences, or related field
  • Willingness to travel regionally for project work

Responsibilities

  • Execute IQ, OQ, and PQ protocols
  • Validate lab systems, equipment, and utilities
  • Collaborate with engineering and validation teams
  • Assist in project scheduling and resource planning
  • Support CQV activities across multiple projects
  • Contribute to GMP/GxP documentation and compliance
  • Take on leadership of validation workstreams

Benefits

  • Hands-on experience with pharma validation projects
  • Pathway to senior validation or project leadership roles
  • Collaboration with experienced engineers in regulated environments
Full Job Description
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

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

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