Senior Quality Manager Jobs in New York
Senior Quality Manager jobs in New York are concentrated in manufacturing, life sciences, food and beverage, and healthcare, with demand at every level from quality engineer through director. The busiest hiring markets are New York City, Buffalo, and Albany, where established employers like Pfizer, Johnson & Johnson, and Regeneron maintain large operations requiring experienced quality leadership. The most in-demand specialties are regulatory compliance, GMP-driven pharmaceutical quality, and ISO-certified manufacturing systems. 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 53 Senior Quality Manager Jobs in New York
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Find Senior Quality Manager JobsSenior Quality Manager Jobs by City in New York
Where New York roles are concentrated, by current openings.
Senior Quality Manager Job Market in New York
A snapshot from current New York openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Manufacturing
- Technology & Software
- Automotive
- Science & Research
What New York Employers Look For
The qualifications that appear most often in senior quality manager jobs across New York.
- Bachelor's degree in engineering, life sciences, or a related technical field required
- ASQ Certified Quality Engineer or Certified Quality Manager credential strongly preferred
- Seven or more years of progressive quality management experience in a regulated industry
- Demonstrated expertise in FDA, GMP, or ISO 9001 compliance frameworks
- Experience leading cross-functional teams and managing quality management systems
- Proficiency with CAPA processes, root cause analysis, and quality audit programs
Senior Quality Manager Jobs in New York: Frequently Asked Questions
How do you become a senior quality manager in New York?
Most senior quality manager roles in New York require a bachelor's degree in engineering, life sciences, or a related field, plus substantial experience in quality systems within a regulated industry. New York does not issue a state license specific to quality management, but employers in pharmaceutical and medical device manufacturing strongly favor candidates holding ASQ certifications such as the Certified Quality Manager or Certified Quality Engineer. Experience with FDA-regulated environments and GMP compliance is especially valued in New York's life sciences corridor.
How much do senior quality managers make in New York?
Senior quality managers in New York earn a median of about $130,470 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $81,960 for the lowest 10% to over $206,450 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire senior quality managers in New York?
Employers hiring senior quality managers in New York right now include NTT DATA, CooperSurgical, and Amneal Pharmaceuticals, based on current listings on Migrate Mate as of October 2026. New York's concentration of pharmaceutical manufacturers, food processors, and medical device companies makes it one of the more consistently active hiring markets for quality leadership in the northeastern United States.
Which New York cities have the most senior quality manager jobs?
New York, Albany, and Hauppauge account for the most senior quality manager openings in New York. New York City dominates due to its density of healthcare systems and corporate headquarters, while Buffalo and Albany draw hiring from large-scale manufacturing operations and life sciences facilities that have long anchored those regional economies.
Are there remote senior quality manager jobs in New York?
Yes, but they're uncommon. Senior quality management work is largely hands-on, requiring physical presence for audits, facility inspections, and production floor oversight, which limits remote availability. About 46% of senior quality manager openings tied to New York are remote or hybrid as of October 2026, and those tend to be in quality systems consulting or supplier quality roles that emphasize documentation and vendor oversight rather than direct site operations.
How can I get hired as a senior quality manager in New York with little or no experience?
The most realistic entry path is securing a quality engineer or quality analyst role at a mid-size manufacturer or regulated facility, then building toward senior responsibilities over time. Large New York employers in the pharmaceutical and food production sectors, including operations in the Hudson Valley and Western New York, regularly bring on quality technicians and coordinators as a pipeline into management. Pursuing an ASQ Certified Quality Improvement Associate credential and gaining hands-on CAPA and audit experience strengthens a candidate's profile considerably for an eventual move into senior roles.
Where can I find and apply to senior quality manager jobs in New York?
You can find and apply to senior quality manager jobs in New York on Migrate Mate, which lists current openings across the state. Find roles that match your background and apply directly to the ones that fit.
See All 53 Senior Quality Manager Jobs in New York
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