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Validation Engineer

Job

Sterling Engineering

Belvidere, IL (In Person)

Full-Time

Posted 2 weeks ago (Updated 3 days ago) • Actively hiring

Expires 7/20/2026

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Job Description

Validation Engineer at Sterling Engineering Validation Engineer at Sterling Engineering in Belvidere, Illinois Posted in 14 days ago.
Type:
full-time
Job Description:
VALIDATION ENGINEER
Belvidere, IL | Direct Hire | Full-Time | Onsite ?
WORK AUTHORIZATION REQUIREMENT
Applicants must be authorized to work in the United States without current or future sponsorship. This employer
DOES NOT
provide: H-1B Sponsorship H-1B Transfers OPT/CPT Sponsorship TN Sponsorship Employment-Based Visa Sponsorship of Any Kind Candidates requiring sponsorship now or in the future will not be considered.
ABOUT THE OPPORTUNITY
Join a growing employee-owned automation company that designs and builds custom high-speed assembly equipment for the: Medical Device Industry Consumer Products Industry Industrial Manufacturing Industry We are seeking a Validation Engineer to support equipment qualification, commissioning, and validation activities for custom automation systems.
RESPONSIBILITIES
Validation & Qualification Develop and execute: Design Qualification (DQ) Installation Qualification (IQ) Operational Qualification (OQ) Performance Qualification (PQ) Testing & Commissioning Support Factory Acceptance Testing (FAT) Support Site Acceptance Testing (SAT) Assist with equipment commissioning activities Documentation Create and maintain: Validation Protocols Qualification Reports Commissioning Documentation Technical Documentation Engineering Collaboration Partner with Engineering teams to develop and review: Functional Design Specifications Software Design Specifications Hardware Design Specifications Vision System Specifications Operator Manuals Compliance & Risk Management Perform Risk Assessments Participate in FMEA Activities Support cGMP Compliance Reviews Maintain validation records within Kneat Gx
QUALIFICATIONS
Required Associate Degree in Engineering Technology, Manufacturing Technology, or related field 3+ years of validation experience in a regulated manufacturing environment Experience with: DQ, IQ, OQ, and PQ Protocols FAT and SAT Activities Engineering Drawings and Technical Documentation cGMP Requirements
APPLY TODAY
If you have experience validating equipment in a regulated manufacturing environment and are looking to join a stable, employee-owned organization, we encourage you to apply.