| Location | Mundelein, IL |
| Industry | Staffing/Employment Agencies |
| Salary | $55–$65 Per Hour |
| Company Size | 500 to 999 employees |
| Year Founded | 1969 |
| Website | http://www.sterling-engineering.com |
Position: Lead Validation Specialist
Type: Contract to hire, no sponsorship available currently, NO third party representation
Duration: 12+ months contract to hire
Location: Mundelein, IL 60060 (regional travel as projects require) onsite daily
Pay rate $55.00 - $65.00 per hour - must be able to accept a permanent position
I am looking for a Lead Validation Specialist coming from the food, biotechnology or pharmaceutical industry that can support commissioning, qualification, and validation (C&Q) initiatives across facilities, utilities, equipment, and automated systems.
This is a hands-on senior validation specialist role with leadership responsibility—ideal for someone who enjoys owning validation strategy, interfacing with clients and auditors, and mentoring junior validation specialists.
OVERVIEW OF RESPONSIBILITIES
• Lead and execute IQ/OQ/PQ activities for facilities, utilities, equipment, control systems, and HVAC
• Conduct cGMP audits, gap assessments, and impact analyses to scope validation work
• Develop system specifications aligned with GAMP and Good Engineering Practices (GEP)
• Author and manage Commissioning & Validation Master Plans (CVMPs)
• Coordinate with OEMs, construction managers, contractors, and end users during commissioning and qualification
• Build and maintain Traceability Matrices (UR/FS/DS → IQ/OQ/PQ)
• Author Summary Reports and defend validation outcomes during audits and inspections
• Lead validation staff and support their professional development
• Manage multiple projects simultaneously, balancing scope, schedule, and quality
QUALIFICATIONS
• Bachelor’s degree in Engineering, Science, or Technical discipline with 5–7 years in an FDA-regulated environment
OR
an Associate degree / military / technician background with 7–10 years regulated industry experience
• Must have working knowledge of FDA regulations, cGMP, and GAMP - Food, Pharma or Biotech industry experience
• Experience reviewing P&IDs, wiring diagrams, HVAC/mechanical drawings, and specifications
must have experience as a Validation Engineer or
• Comfortable using field measurement and verification instrumentation
• Excellent technical writing, communication, and client-facing skills
• Proven ability to manage scope, change control, and problem resolution
Sterling Engineering has been a trusted partner for engineering, project management, and staffing solutions for over five decades. We provide exceptional engineering/technical recruitment and engineering project services to clients nationwide:
Sterling offers a unique combination of engineering solutions and Best of Staffing level service to help our clients and talent achieve their goals.