QA Manager Jobs in New York
QA Manager jobs in New York are in strong demand, concentrated in the pharmaceutical and biotech corridor along the Hudson Valley, financial services technology on Wall Street, and the fast-growing healthcare systems across all five boroughs and Long Island. Most hiring activity centers on New York City, Buffalo, and Albany, where employers like Pfizer, Citigroup, and Memorial Sloan Kettering maintain large quality and compliance teams. Openings run the full seniority range, from associate qa manager roles through senior quality directors, with the deepest need in software QA, regulatory compliance, and clinical 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
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 plasma products.
- 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.
- Draft protocols for new and existing instruments and processes within the lab.
- Monitor plasma centers for compliance with customer requirements.
- Ensure proper storage and documentation of supplies, reagents, and equipment.
- Perform quality control checks on stored and shipped products, as well as test reagents.
- Perform reviews of completed runs and changes in supply lots.
- 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.
- 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 two years’ experience in a laboratory setting 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
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 plasma products.
- 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.
- Draft protocols for new and existing instruments and processes within the lab.
- Monitor plasma centers for compliance with customer requirements.
- Ensure proper storage and documentation of supplies, reagents, and equipment.
- Perform quality control checks on stored and shipped products, as well as test reagents.
- Perform reviews of completed runs and changes in supply lots.
- 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.
- 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 two years’ experience in a laboratory setting 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 115+ QA Manager Jobs in New York
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Find QA Manager JobsQA Manager Jobs by City in New York
Where New York roles are concentrated, by current openings.
QA Manager Job Market in New York
A snapshot from current New York openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Technology & Software
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
- Retail
- Consumer Goods
What New York Employers Look For
The qualifications that appear most often in QA manager jobs across New York.
- Bachelor's degree in engineering, computer science, life sciences, or a related technical field
- Five or more years of quality assurance experience including team leadership or supervisory responsibility
- Demonstrated experience with quality management systems such as ISO 9001, FDA 21 CFR, or CMMI
- Proficiency with test management tools such as JIRA, TestRail, or comparable enterprise platforms
- Working knowledge of Agile and Scrum methodologies as applied to QA processes
- Strong written communication skills for preparing quality reports, SOPs, and audit documentation
QA Manager Jobs in New York: Frequently Asked Questions
How do you become a qa manager in New York?
Most qa managers in New York reach the role through a combination of a bachelor's degree in a technical field and several years of hands-on QA experience, followed by a move into team leadership. New York does not require a state-issued license specifically for qa managers, but employers in regulated industries such as pharmaceuticals and medical devices expect familiarity with FDA quality system regulations. Certifications like ASQ's Certified Quality Manager are widely respected across New York hiring markets and can accelerate promotion from individual contributor to manager.
Which companies hire qa managers in New York?
Employers hiring qa managers in New York right now include Saputo, NTT DATA, and Moog, based on current listings on Migrate Mate as of October 2026. New York's concentration of pharmaceutical manufacturers, financial technology firms, and large hospital networks means demand holds consistently across multiple industries rather than clustering in a single sector.
Which New York cities have the most qa manager jobs?
The cities with the most qa manager openings in New York are New York, Rochester, and Albany. New York City dominates volume because of its density of financial services, media, and healthcare employers, while Buffalo's growing advanced manufacturing base and Albany's pharmaceutical and government technology sectors drive meaningful hiring in those upstate markets.
Are there remote qa manager jobs in New York?
Yes, and more than many management roles, particularly for qa managers working in software, data, or financial technology. About 32% of qa manager openings tied to New York are remote or hybrid as of October 2026, reflecting how much of the work involves reviewing documentation, managing testing pipelines, and coordinating distributed teams. Roles tied to physical manufacturing lines, clinical environments, or regulated lab settings remain primarily on-site.
How can I get hired as a qa manager in New York with little or no experience?
The most realistic entry path is moving into a QA analyst or quality assurance engineer role first, then building toward management. Large New York employers in pharma and healthcare, including hospital systems across the city's five boroughs and manufacturers in the Hudson Valley, regularly hire junior quality associates with a relevant degree and entry-level certifications like ASQ's Certified Quality Improvement Associate. Gaining experience with FDA-regulated processes or agile software testing environments makes candidates from adjacent roles such as project coordinator or business analyst much more competitive for an eventual qa manager promotion.
Where can I find and apply to qa manager jobs in New York?
You can find and apply to qa manager jobs in New York on Migrate Mate, which lists current openings across New York City, Buffalo, Albany, and the surrounding region. Find roles that match your experience and apply directly to the ones that fit.
See All 115+ QA Manager Jobs in New York
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