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Biotech Validation Jobs in Chicago, IL (NOW HIRING)

Senior Engineer, Process Validation

Chicago, IL · On-site +1

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... The Senior Engineer, Process Validation is responsible for leading & supporting internal and ...

Senior Engineer, Process Validation

Chicago, IL · On-site +1

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... The Senior Engineer, Process Validation is responsible for leading & supporting internal and ...

... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...

... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...

... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...

Quality Engineer - Validation

Buffalo Grove, IL · On-site

$73K - $95K/yr

... for the pharmaceutical, biotechnology and generic industries. We leverage a long-standing ... The Quality Validation Engineer is responsible for planning, coordinating and managing through ...

Quality Engineer - Validation

Buffalo Grove, IL · On-site

$73K - $95K/yr

... for the pharmaceutical, biotechnology and generic industries. We leverage a long-standing ... The Quality Validation Engineer is responsible for planning, coordinating and managing through ...

Senior Process Facilities Engineer

Chicago, IL · On-site

$107K - $138K/yr

  • Medical

  • Life

  • Retirement

... Validation Services to the Pharmaceutical, Biotechnology, Biologics, and Medical Device industries. VTI offers professional development, training, competitive compensation, excellent benefits, a ...

Senior Process Facilities Engineer

Chicago, IL · On-site

$107K - $138K/yr

  • Medical

  • Life

  • Retirement

... Validation Services to the Pharmaceutical, Biotechnology, Biologics, and Medical Device industries. VTI offers professional development, training, competitive compensation, excellent benefits, a ...

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Biotech Validation information

See Chicago, IL salary details

$23

$53

$80

How much do biotech validation jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for biotech validation in Chicago, IL is $53.56, according to ZipRecruiter salary data. Most workers in this role earn between $40.62 and $65.14 per hour, depending on experience, location, and employer.

What job categories do people searching Biotech Validation jobs in Chicago, IL look for?

The top searched job categories for Biotech Validation jobs in Chicago, IL are:

Infographic showing various Biotech Validation job openings in Chicago, IL as of July 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $111,413 per year, or $53.6 per hour.

Lead Validation Specialist

Sterling Engineering Inc.

Mundelein, IL

$55 - $65/hr

Contractor

Posted 8 days ago


Job description

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


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.