SE
Validation Engineer-Belvedere
Accepting applicationsSterling Engineering · South Elgin, IL
Full-Time Mid_senior aiateganrf
Posted
1d ago
Category
Test
Experience
Mid_senior
Country
United States
Validation Engineer
Belvidere, IL | ?Up to $100K | Employee-Owned Company
(DIRECT HIRE)
No Visa Transfers nor Visa Sponsorship
Join a growing automation manufacturer where your work directly impacts the medical device and advanced manufacturing industries.
Our client is a 100% employee-owned engineering company specializing in the design and build of custom high-speed automation assembly systems used in medical device, consumer goods, and industrial manufacturing environments. They are seeking a hands-on Validation Engineer to support commissioning, qualification, and technical documentation efforts for complex automated machinery.
This is a fully onsite opportunity in Belvidere, IL with occasional travel to the South Elgin facility as needed.
What You’ll Be Doing
Develop and execute DQ/IQ/OQ/PQ validation protocols in compliance with cGMP standards
Support FAT and SAT commissioning & qualification activities with customers
Create and maintain technical documentation including:
Functional Design Specifications
Software & Hardware Design Specs
Configuration & Vision Specs
Technical Manuals & Operator Guides
Machine Instructions & Spare Parts Documentation
Execute machine test cases to verify functionality and quality performance
Update validation documentation in Kneat Gx
Conduct risk assessments and FMEA activities
Support CE technical construction file development
What They’re Looking For
2-year technical degree in engineering or related field
3+ years of experience writing technical documentation in manufacturing environments
Experience with validation protocols and commissioning activities
Ability to read blueprints and develop technical documents
Experience with cGMP environments preferred
LEAN, Six Sigma, ISO, or medical device experience is a plus
Why This Opportunity Stands Out
Employee Stock Ownership Program (ESOP)
Pension Plan + 401(k) Contribution
Excellent medical benefits
Employer-paid dental, vision, disability & life insurance
Tuition reimbursement
Wellness reimbursement
Stable, growing organization with cutting-edge automation projects
Flexible Friday schedule (half days!)
Schedule: Monday-Thursday 7AM-4PM | Friday 7AM-12PM
Compensation: $72K-$100K depending on experience
Screening Questions
Do you have experience writing and executing DQ/IQ/OQ/PQ validation protocols in a cGMP environment?
Have you participated in FAT and SAT activities for manufacturing equipment?
Do you have experience creating technical documentation such as FDS, SDS, HDS, validation protocols, or operator manuals?
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.
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Belvidere, IL | ?Up to $100K | Employee-Owned Company
(DIRECT HIRE)
No Visa Transfers nor Visa Sponsorship
Join a growing automation manufacturer where your work directly impacts the medical device and advanced manufacturing industries.
Our client is a 100% employee-owned engineering company specializing in the design and build of custom high-speed automation assembly systems used in medical device, consumer goods, and industrial manufacturing environments. They are seeking a hands-on Validation Engineer to support commissioning, qualification, and technical documentation efforts for complex automated machinery.
This is a fully onsite opportunity in Belvidere, IL with occasional travel to the South Elgin facility as needed.
What You’ll Be Doing
Develop and execute DQ/IQ/OQ/PQ validation protocols in compliance with cGMP standards
Support FAT and SAT commissioning & qualification activities with customers
Create and maintain technical documentation including:
Functional Design Specifications
Software & Hardware Design Specs
Configuration & Vision Specs
Technical Manuals & Operator Guides
Machine Instructions & Spare Parts Documentation
Execute machine test cases to verify functionality and quality performance
Update validation documentation in Kneat Gx
Conduct risk assessments and FMEA activities
Support CE technical construction file development
What They’re Looking For
2-year technical degree in engineering or related field
3+ years of experience writing technical documentation in manufacturing environments
Experience with validation protocols and commissioning activities
Ability to read blueprints and develop technical documents
Experience with cGMP environments preferred
LEAN, Six Sigma, ISO, or medical device experience is a plus
Why This Opportunity Stands Out
Employee Stock Ownership Program (ESOP)
Pension Plan + 401(k) Contribution
Excellent medical benefits
Employer-paid dental, vision, disability & life insurance
Tuition reimbursement
Wellness reimbursement
Stable, growing organization with cutting-edge automation projects
Flexible Friday schedule (half days!)
Schedule: Monday-Thursday 7AM-4PM | Friday 7AM-12PM
Compensation: $72K-$100K depending on experience
Screening Questions
Do you have experience writing and executing DQ/IQ/OQ/PQ validation protocols in a cGMP environment?
Have you participated in FAT and SAT activities for manufacturing equipment?
Do you have experience creating technical documentation such as FDS, SDS, HDS, validation protocols, or operator manuals?
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.
Show more Show less