QA Manager Jobs in Illinois
QA Manager jobs in Illinois are in strong demand, concentrated in manufacturing, life sciences, food processing, and software development, with openings at every level from associate qa manager through director of quality. Chicago, Peoria, and Rockford are the busiest hiring markets, home to established employers like Abbott Laboratories, Caterpillar, and Deere and Company, all of which maintain substantial quality functions across their Illinois facilities. The most sought-after specialties include quality management systems, regulatory compliance, and software quality assurance. 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 100 QA Manager Jobs in Illinois
Find roles in Illinois that match your experience and apply in just a few clicks.
Find QA Manager JobsQA Manager Jobs by City in Illinois
Where Illinois roles are concentrated, by current openings.
QA Manager 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 manager jobs across Illinois.
- Bachelor's degree in engineering, life sciences, or a related technical field required
- Demonstrated experience managing quality systems such as ISO 9001 or AS9100
- Proficiency with statistical process control tools and root cause analysis methods
- Familiarity with Illinois-relevant regulatory frameworks including FDA 21 CFR for life sciences roles
- Experience leading cross-functional teams and managing direct reports in a quality function
- Certification such as ASQ Certified Manager of Quality and Organizational Excellence preferred
QA Manager Jobs in Illinois: Frequently Asked Questions
How do you become a qa manager in Illinois?
Most qa manager roles in Illinois require a bachelor's degree in engineering, life sciences, business, or a related field, followed by several years of hands-on quality experience. Illinois does not issue a state license specific to qa managers, but employers across manufacturing and life sciences strongly prefer candidates who hold ASQ credentials, particularly the Certified Manager of Quality and Organizational Excellence. Building experience in regulated industries like medical devices or food processing significantly strengthens a candidacy in this market.
Which companies hire qa managers in Illinois?
Employers hiring qa managers in Illinois right now include GEI Consultants, Medline Industries, and AbbVie, based on current listings on Migrate Mate as of August 2026. Illinois's concentration of pharmaceutical manufacturers, automotive suppliers, and food and beverage companies means qa manager demand is distributed across a wide range of industries statewide.
Which Illinois cities have the most qa manager jobs?
Chicago, Niles, and Waukegan have the most qa manager openings in Illinois. Chicago dominates because of its density of corporate headquarters, medical device firms, and technology companies, while Peoria and Rockford draw significant demand from heavy manufacturing and industrial equipment employers like Caterpillar and its broader supplier network that anchor those regional economies.
Are there remote qa manager jobs in Illinois?
Yes, but they're less common than in purely desk-based fields, since many qa manager roles involve overseeing physical production lines, labs, or on-site audits. About 27% of qa manager openings tied to Illinois are remote or hybrid as of August 2026, which reflects a meaningful but selective portion of the market. The parts of the role most suited to remote work include documentation review, supplier audits conducted digitally, and quality management system oversight.
How can I get hired as a qa manager in Illinois with little or no experience?
The most realistic entry path is moving into a qa coordinator or quality technician role first, then building toward management. Large Illinois manufacturers and life sciences companies, including those in the Chicago metro and along the I-90 corridor, regularly hire quality inspectors and associates who can grow internally. Earning an entry-level ASQ certification such as the Certified Quality Technician demonstrates seriousness to Illinois employers and provides a concrete edge over other candidates without a long quality resume.
Where can I find and apply to qa manager jobs in Illinois?
You can find and apply to qa manager jobs in Illinois on Migrate Mate, which lists current openings from employers actively hiring across the state. Find roles that match your experience and apply directly to the ones that fit.
See All 100 QA Manager Jobs in Illinois
Find roles in Illinois that match your experience and apply in just a few clicks.
Find QA Manager Jobs