Quality Assurance Lead Jobs in New York
Quality Assurance Lead jobs in New York are consistently active, with strong demand concentrated in pharmaceuticals, financial services, technology, and consumer goods manufacturing. New York City, Buffalo, and Albany are the largest hiring metros for this role, and employers such as Pfizer, JPMorgan Chase, and IBM regularly bring on quality assurance leads at levels from junior to senior program oversight. The most in-demand specialties are software quality assurance, pharmaceutical compliance QA, and financial services audit readiness. 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 113+ Quality Assurance Lead Jobs in New York
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Find Quality Assurance Lead JobsQuality Assurance Lead Jobs by City in New York
Where New York roles are concentrated, by current openings.
Quality Assurance Lead 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 quality assurance lead jobs across New York.
- Bachelor's degree in a relevant field such as engineering, computer science, or life sciences
- Three or more years of quality assurance experience with demonstrated leadership responsibilities
- Proficiency with QA methodologies including Agile, SDLC, or GMP depending on the industry
- Experience writing and executing test plans, test cases, and defect reports
- Familiarity with industry-specific regulatory frameworks such as FDA 21 CFR Part 11 or ISO 9001
- Strong communication skills to coordinate across cross-functional teams and present findings to management
Quality Assurance Lead Jobs in New York: Frequently Asked Questions
How do you become a quality assurance lead in New York?
Most quality assurance lead roles in New York require a bachelor's degree in engineering, computer science, life sciences, or a related field, combined with progressive QA experience. There is no state-issued license specific to the role, but industry certifications such as the Certified Quality Engineer or Certified Software Quality Engineer from the American Society for Quality are widely recognized by New York employers and give candidates a meaningful competitive edge when applying.
How much do quality assurance leads make in New York?
Quality assurance leads in New York earn a median of about $121,240 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $58,180 for the lowest 10% to over $182,910 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire quality assurance leads in New York?
Employers hiring quality assurance leads 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 dense mix of pharmaceutical manufacturers, financial institutions, and enterprise technology firms means demand for this role is distributed across multiple industries rather than concentrated in one sector.
Which New York cities have the most quality assurance lead jobs?
New York, Rochester, and Albany have the most quality assurance lead openings in New York. New York City leads due to its concentration of financial services firms, tech companies, and large corporate headquarters, while Buffalo and Albany generate demand through pharmaceutical manufacturing, state government operations, and regional healthcare systems that maintain dedicated quality functions.
Are there remote quality assurance lead jobs in New York?
Yes, and more than many comparable leadership roles. About 34% of quality assurance lead openings tied to New York are remote or hybrid as of October 2026, reflecting how much of the work centers on documentation, test planning, and cross-team coordination rather than physical inspection. Software and financial services QA roles are the most likely to offer fully remote arrangements.
How can I get hired as a quality assurance lead in New York with little or no experience?
The most realistic entry path is moving into a quality assurance analyst or QA tester role first, then building toward a lead position over time. Large New York employers in pharma and finance often hire entry-level QA associates who rotate through testing, documentation, and compliance functions before advancing. Earning a Certified Associate in Software Quality or completing a QA bootcamp recognized by New York tech employers helps candidates without a formal background stand out when applying to analyst roles that feed into lead tracks.
Where can I find and apply to quality assurance lead jobs in New York?
You can find and apply to quality assurance lead jobs in New York on Migrate Mate, which lists current openings in the state. Find roles that fit your experience and location, then apply directly to each one through the listing.
See All 113+ Quality Assurance Lead Jobs in New York
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