Mundelein, IL · On-site
$55 - $65/hr
... biotechnology or pharmaceutical industry that can support commissioning, qualification, and validation (C&Q) initiatives across facilities, utilities, equipment, and automated systems. This is a ...
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Mundelein, IL · On-site
$55 - $65/hr
... biotechnology or pharmaceutical industry that can support commissioning, qualification, and validation (C&Q) initiatives across facilities, utilities, equipment, and automated systems. This is a ...
Mount Prospect, IL · On-site
Minimum of 5 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries. * Proficient knowledge of cleaning validation, continuous process improvement ...
Mount Prospect, IL · On-site
Minimum of 5 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries. * Proficient knowledge of cleaning validation, continuous process improvement ...
Mount Prospect, IL · On-site
Minimum of 5 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries. * Proficient knowledge of cleaning validation, continuous process improvement ...
Mount Prospect, IL · On-site
Minimum of 5 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries. * Proficient knowledge of cleaning validation, continuous process improvement ...
Key Responsibilities Validation Services * Perform autoclave qualification and validation ... Experience in pharmaceutical, biotechnology, healthcare, research laboratory, or regulated ...
Key Responsibilities Validation Services * Perform autoclave qualification and validation ... Experience in pharmaceutical, biotechnology, healthcare, research laboratory, or regulated ...
Key Responsibilities Validation Services * Perform autoclave qualification and validation ... Experience in pharmaceutical, biotechnology, healthcare, research laboratory, or regulated ...
Key Responsibilities Validation Services * Perform autoclave qualification and validation ... Experience in pharmaceutical, biotechnology, healthcare, research laboratory, or regulated ...
IL · On-site
Experience in Manufacturing Validation, CQV, Equipment Qualification, or Process Validation within the pharmaceutical, biotechnology, or medical device industry. * Hands-on experience performing IQ ...
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IL · On-site
Experience in Manufacturing Validation, CQV, Equipment Qualification, or Process Validation within the pharmaceutical, biotechnology, or medical device industry. * Hands-on experience performing IQ ...
Rosemont, IL · On-site
$42K - $47K/yr
Proteintech is a fast-growing Biotech company located in the greater Chicago area. Our Mission is ... validation, and QC process. 200,000+ citations of Proteintech products demonstrates what matters ...
Rosemont, IL · On-site
$42K - $47K/yr
Proteintech is a fast-growing Biotech company located in the greater Chicago area. Our Mission is ... validation, and QC process. 200,000+ citations of Proteintech products demonstrates what matters ...
Chicago, IL · On-site
$70K - $100K/yr
CQV (Commissioning, Qualification, Validation) * or GMP-regulated environments (Pharma / Biotech) * Strong understanding of: * GMP / GxP / FDA regulations * Validation lifecycle (IQ/OQ/PQ) * Ability ...
Chicago, IL · On-site
$70K - $100K/yr
CQV (Commissioning, Qualification, Validation) * or GMP-regulated environments (Pharma / Biotech) * Strong understanding of: * GMP / GxP / FDA regulations * Validation lifecycle (IQ/OQ/PQ) * Ability ...
Waukegan, IL · On-site
$60 - $75/hr
Position: Sr Validation Engineer Location: Waukegan, IL 60087 onsite 5 days a week Duration: 1 2+ ... ADC or biotechnology manufacturing experience. * Experience with single-use systems, single-use ...
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Waukegan, IL · On-site
$60 - $75/hr
Position: Sr Validation Engineer Location: Waukegan, IL 60087 onsite 5 days a week Duration: 1 2+ ... ADC or biotechnology manufacturing experience. * Experience with single-use systems, single-use ...
Gurnee, IL · On-site
$70 - $110/hr
Industry Pharma/Biotech/Clinical Research * City Gurnee * Country United States Location: Gurnee ... This is an excellentopportunity for a validation professional with approximately 3-5 years ...
Gurnee, IL · On-site
$70 - $110/hr
Industry Pharma/Biotech/Clinical Research * City Gurnee * Country United States Location: Gurnee ... This is an excellentopportunity for a validation professional with approximately 3-5 years ...
Round Lake, IL · On-site
$96K - $132K/yr
... biotechnology, or medical device manufacturing. * Strong knowledge of validation lifecycle management, computerized systems, data integrity principles, risk management, and applicable regulatory ...
Round Lake, IL · On-site
$96K - $132K/yr
... biotechnology, or medical device manufacturing. * Strong knowledge of validation lifecycle management, computerized systems, data integrity principles, risk management, and applicable regulatory ...
Round Lake, IL · On-site
$96K - $132K/yr
... biotechnology, or medical device manufacturing. * Strong knowledge of validation lifecycle management, computerized systems, data integrity principles, risk management, and applicable regulatory ...
Round Lake, IL · On-site
$96K - $132K/yr
... biotechnology, or medical device manufacturing. * Strong knowledge of validation lifecycle management, computerized systems, data integrity principles, risk management, and applicable regulatory ...
Chicago, IL · On-site +1
$100K - $130K/yr
... 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 ...
Chicago, IL · On-site +1
$100K - $130K/yr
... 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 ...
Chicago, IL · On-site +1
$100K - $130K/yr
... 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 ...
Chicago, IL · On-site +1
$100K - $130K/yr
... 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 ...
Chicago, IL · On-site +1
... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...
Chicago, IL · On-site +1
... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...
Chicago, IL · On-site +1
... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...
Chicago, IL · On-site +1
... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...
Chicago, IL · On-site +1
... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...
Chicago, IL · On-site +1
... pharma, biotech, medical device, or clinical * Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements ...
Chicago, IL · On-site +1
It provides process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. For projects of every scale, we ...
Chicago, IL · On-site +1
It provides process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. For projects of every scale, we ...
Chicago, IL · On-site
$110 - $150/hr
... validation , commissioning , or qualification activities within GMP-regulated pharmaceutical or biotech manufacturing environments * Strong understanding of cGMP requirements, FDA regulations ...
Chicago, IL · On-site
$110 - $150/hr
... validation , commissioning , or qualification activities within GMP-regulated pharmaceutical or biotech manufacturing environments * Strong understanding of cGMP requirements, FDA regulations ...
Prepare and execute validation plans, User Requirements Specifications, functional and design ... Experience working in pharmaceutical, biotechnology, medical-device, or another highly regulated ...
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Prepare and execute validation plans, User Requirements Specifications, functional and design ... Experience working in pharmaceutical, biotechnology, medical-device, or another highly regulated ...
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$55 - $65/hr
Contractor
Posted 29 days ago
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
