QA Lead Jobs in Illinois
QA Lead jobs in Illinois are in consistent demand across the state's technology, manufacturing, financial services, and healthcare sectors, with openings at every level from junior lead through senior quality director. Chicago, Schaumburg, and Deerfield anchor most of the hiring, where established employers like Motorola Solutions, Baxter International, and Discover Financial Services maintain substantial quality engineering teams. The most in-demand specialties in Illinois listings include automation testing, Agile QA process ownership, and regulated-industry compliance validation. Find a role that fits below and apply directly.
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KEDPLASMA is a subsidiary of Kedrion Biopharma Inc. KEDPLASMA specializes in the collection and procurement of high-quality plasma that is processed into plasma-based therapies. Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Our therapies help treat and prevent serious diseases, including Hemophilia, Primary Immune System Deficiencies, and Rh-Sensitization.
Job Summary
Are you detail-oriented and passionate about quality and compliance? Join our team as a Quality Assurance Specialist and help ensure the safety and integrity of life-saving plasma products. In this role, you’ll be a key player in upholding regulatory standards and supporting continuous improvement across the center’s operations.
As a Quality Assurance Specialist, you’ll work closely with the Quality Assurance Manager and center leadership to monitor compliance, review documentation, and support training and audit readiness. Your work will directly impact donor safety and product quality.
What you'll do
- Review manufacturing activities and documentation to ensure compliance with SOPs and regulatory requirements.
- Identify and escalate non-compliance issues that could affect donor safety or plasma quality.
- Support plasma release and shipment processes, ensuring all units meet specifications.
- Investigate deviations and assist in implementing corrective actions.
- Audit records for completeness, consistency, and accuracy to maintain data integrity.
- Monitor equipment qualification, calibration, and maintenance documentation.
- Ensure proper storage and documentation of supplies, reagents, and equipment.
- Perform quality control checks on stored and shipped products, as well as test reagents.
- Track and trend quality data to identify improvement opportunities.
- Participate in internal audits and support external inspections.
- Assist in training staff on quality procedures and ensure training records are up to date.
- Evaluate staff competency through direct observation, written assessments, and proficiency testing.
- Prepare and submit epidemiological data and compliance reports as required.
- Promote a culture of continuous improvement and regulatory excellence.
Qualifications and need-to-know
- Bachelor’s degree in life sciences or a related field preferred.
- Minimum 1 year of experience in a regulated industry (plasma center or biomedical field preferred).
- Ability to analyze data and identify trends.
- Strong organizational and documentation skills.
- Familiarity with FDA, EU GMP, and cGMP standards.
- Excellent communication and collaboration skills.
- Comfortable working in a highly regulated environment with exposure to bloodborne pathogens and cold storage areas.
- Proficiency in Microsoft Office and data entry systems preferred.
Employment eligibility verification will be required at the time of hire. This position does not offer visa sponsorship now or in the future.
Kedrion Biopharma Inc. is committed to providing equal employment opportunities to all employees and applicants. We prohibit discrimination and harassment based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all employment terms, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Salary ranges are determined based on relevant experience, education, and certifications.
If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at kedtalent@kedrion.com.
Employee Benefits: At Kedrion Biopharma Inc., we believe in taking care of our people. Our benefits package is designed to support your health, happiness, and future, including:
- Health & Wellness – Full medical, dental, and vision coverage
- Financial Security – Life insurance, AD&D, and retirement savings plans
- Work-Life Balance – Paid time off, sick leave, and paid holidays
- Career Growth – Training programs and development opportunities
- Extra Perks – Employee discounts, wellness initiatives, and more!
For specific inquiries please reach out to us
Kedrion Biopharma Inc. participates in E-Verify and provides the federal government with Form I-9 information to confirm employment authorization. For more information, please contact the Department of Homeland Security.
KEDPLASMA is a subsidiary of Kedrion Biopharma Inc. KEDPLASMA specializes in the collection and procurement of high-quality plasma that is processed into plasma-based therapies. Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Our therapies help treat and prevent serious diseases, including Hemophilia, Primary Immune System Deficiencies, and Rh-Sensitization.
Job Summary
Are you detail-oriented and passionate about quality and compliance? Join our team as a Quality Assurance Specialist and help ensure the safety and integrity of life-saving plasma products. In this role, you’ll be a key player in upholding regulatory standards and supporting continuous improvement across the center’s operations.
As a Quality Assurance Specialist, you’ll work closely with the Quality Assurance Manager and center leadership to monitor compliance, review documentation, and support training and audit readiness. Your work will directly impact donor safety and product quality.
What you'll do
- Review manufacturing activities and documentation to ensure compliance with SOPs and regulatory requirements.
- Identify and escalate non-compliance issues that could affect donor safety or plasma quality.
- Support plasma release and shipment processes, ensuring all units meet specifications.
- Investigate deviations and assist in implementing corrective actions.
- Audit records for completeness, consistency, and accuracy to maintain data integrity.
- Monitor equipment qualification, calibration, and maintenance documentation.
- Ensure proper storage and documentation of supplies, reagents, and equipment.
- Perform quality control checks on stored and shipped products, as well as test reagents.
- Track and trend quality data to identify improvement opportunities.
- Participate in internal audits and support external inspections.
- Assist in training staff on quality procedures and ensure training records are up to date.
- Evaluate staff competency through direct observation, written assessments, and proficiency testing.
- Prepare and submit epidemiological data and compliance reports as required.
- Promote a culture of continuous improvement and regulatory excellence.
Qualifications and need-to-know
- Bachelor’s degree in life sciences or a related field preferred.
- Minimum 1 year of experience in a regulated industry (plasma center or biomedical field preferred).
- Ability to analyze data and identify trends.
- Strong organizational and documentation skills.
- Familiarity with FDA, EU GMP, and cGMP standards.
- Excellent communication and collaboration skills.
- Comfortable working in a highly regulated environment with exposure to bloodborne pathogens and cold storage areas.
- Proficiency in Microsoft Office and data entry systems preferred.
Employment eligibility verification will be required at the time of hire. This position does not offer visa sponsorship now or in the future.
Kedrion Biopharma Inc. is committed to providing equal employment opportunities to all employees and applicants. We prohibit discrimination and harassment based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all employment terms, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Salary ranges are determined based on relevant experience, education, and certifications.
If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at kedtalent@kedrion.com.
Employee Benefits: At Kedrion Biopharma Inc., we believe in taking care of our people. Our benefits package is designed to support your health, happiness, and future, including:
- Health & Wellness – Full medical, dental, and vision coverage
- Financial Security – Life insurance, AD&D, and retirement savings plans
- Work-Life Balance – Paid time off, sick leave, and paid holidays
- Career Growth – Training programs and development opportunities
- Extra Perks – Employee discounts, wellness initiatives, and more!
For specific inquiries please reach out to us
Kedrion Biopharma Inc. participates in E-Verify and provides the federal government with Form I-9 information to confirm employment authorization. For more information, please contact the Department of Homeland Security.
See All 97 QA Lead Jobs in Illinois
Find roles in Illinois that match your experience and apply in just a few clicks.
Find QA Lead JobsQA Lead Jobs by City in Illinois
Where Illinois roles are concentrated, by current openings.
QA Lead Job Market in Illinois
A snapshot from current Illinois openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Consulting & Professional Services
- Manufacturing
- Electronics & Hardware
- Biotechnology & Pharmaceuticals
- Education
What Illinois Employers Look For
The qualifications that appear most often in QA lead jobs across Illinois.
- Bachelor's degree in computer science, engineering, or a related technical field required
- Three or more years of quality assurance experience with demonstrated team leadership
- Proficiency in test automation frameworks such as Selenium, Cypress, or Appium
- Experience with Agile or Scrum methodologies and sprint-based QA planning
- Strong knowledge of SDLC, defect tracking tools, and CI/CD pipeline integration
- Excellent communication skills for cross-functional collaboration with product and development teams
QA Lead Jobs in Illinois: Frequently Asked Questions
How do you become a qa lead in Illinois?
Most qa leads in Illinois start with a bachelor's degree in computer science, information technology, or engineering, then build several years of hands-on QA experience before moving into a lead role. Illinois does not require a state-issued license for quality assurance work, but industry certifications such as ISTQB or CSTE are widely recognized by Illinois employers and can accelerate advancement. Demonstrating experience leading test cycles and mentoring junior testers is the clearest path to lead-level hiring in this state.
Which companies hire qa leads in Illinois?
Employers hiring qa leads in Illinois right now include GEI Consultants, AbbVie, and Abbott, based on current listings on Migrate Mate as of August 2026. Illinois's density of technology firms, financial institutions, and regulated manufacturers in the Chicago metro area means demand for experienced qa leads remains broad across multiple industries.
Which Illinois cities have the most qa lead jobs?
The cities with the most qa lead openings in Illinois are Chicago, Niles, and Waukegan. Chicago drives the largest share of postings due to its concentration of enterprise technology companies, financial services firms, and healthcare systems, while suburban hubs like Schaumburg and Deerfield contribute meaningfully because of the major corporate headquarters and manufacturing operations anchored there.
Are there remote qa lead jobs in Illinois?
Yes, and more than many fields, since qa lead work is primarily desk-based, analytical, and executable through remote collaboration tools. About 21% of qa lead openings tied to Illinois are remote or hybrid as of August 2026, reflecting the role's strong compatibility with distributed teams. Test planning, defect triage, and team coordination are the parts of the role most commonly performed remotely.
How can I get hired as a qa lead in Illinois with little or no experience?
The most realistic entry path is landing a QA analyst or software tester role first, then building toward lead responsibilities. Large Illinois employers in financial services and healthcare technology frequently hire associate QA testers or junior automation engineers without requiring prior lead experience. Earning an ISTQB Foundation certification gives candidates a competitive edge in Illinois listings. From a QA analyst role, volunteering to coordinate test plans or mentor newer teammates is the practical route to a formal lead title.
Where can I find and apply to qa lead jobs in Illinois?
You can find and apply to qa lead jobs in Illinois on Migrate Mate, which lists current Illinois openings updated regularly. Find the roles that fit your experience and apply directly to the employers posting them.
See All 97 QA Lead Jobs in Illinois
Find roles in Illinois that match your experience and apply in just a few clicks.
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