QA Analyst Jobs in Chicago, IL
QA Analyst jobs in Chicago are concentrated in the Loop, River North, and the Fulton Market tech corridor, where demand runs across fintech, enterprise software, and healthcare IT. Employers hiring right now include Jobot, BRAVEN, and Tempus. Scan the live roles below and apply to whichever ones fit.
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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 Analyst Jobs in Chicago
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Who's Hiring
Top Industries Hiring
- Education
- Manufacturing
- Staffing & Recruiting
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
QA Analyst Jobs in Chicago: Frequently Asked Questions
How do I get a qa analyst job in Chicago?
Focus your search on Chicago's fintech corridor along LaSalle Street, the enterprise software companies clustered in the Loop and River North, and the major health systems anchored on the Near North Side. Candidates with hands-on experience in automated testing frameworks and agile workflows stand out. Networking through local tech meetups and Chicago-based product communities also surfaces openings before they hit job boards.
Which companies hire qa analysts in Chicago?
Companies currently hiring qa analysts in Chicago include Jobot, BRAVEN, and Tempus, per current listings on Migrate Mate as of August 2026. Chicago's mix of legacy financial institutions, fast-growing fintech startups, and large healthcare organizations means demand comes from a wide range of employer sizes and industries.
Are there remote qa analyst jobs in Chicago?
Yes, qa analyst work is well-suited to remote and hybrid arrangements because most testing and defect tracking happens through software tools rather than on-site hardware. About 22% of qa analyst openings tied to Chicago are remote or hybrid as of August 2026, reflecting the desk-based nature of the role. Automation QA and software testing positions tend to be the most remote-friendly, while roles requiring device or hardware validation are more likely to require on-site presence.
How can I get a qa analyst job in Chicago with little or no experience?
The most realistic entry path in Chicago is targeting junior QA or software tester roles at mid-size startups in Fulton Market or River North, where teams are smaller and entry-level candidates get broader exposure faster. Community college certificate programs in software testing and bootcamp graduates find traction with Chicago's growing fintech and health tech employers. Building a portfolio of documented test cases, even from personal or open-source projects, gives hiring managers something concrete to evaluate.
Which industries hire the most qa analysts in Chicago?
Most qa analyst openings in Chicago sit in Education, Manufacturing, and Staffing & Recruiting, per current listings on Migrate Mate as of August 2026. Chicago's deep roots in financial services, its expanding health tech sector centered on the Near North Side medical corridor, and its growing base of enterprise software firms all drive consistent demand for quality assurance professionals.
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