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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Showing 5 of 104+ QA Manager jobs
Description:
The QA Inspector monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run.
Essential Functions:
- Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. Preparation of samples for chemical and microbiological (where required) analysis and delivering them to the QC lab. Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance to specifications. Maintaining detailed records of sampling, inspections and testing activities. Assigning and verification of expiry date and retest date for all the GMP raw materials through vendor COA and in-house COA. Collection of packaged product samples for annual stability.
- Perform room, equipment, and packaging line checks (where applicable) prior to each stage of manufacturing following detailed written procedures. Conduct in process testing per manufacturing and packaging batch record instructions. Prepare controlled / uncontrolled / packaged finished product samples for QC lab and QA retains, following detailed documentation procedures. Maintenance of standard weights required to perform daily verification of balances.
- Labeling component receipt, visual examination, counting, preliminary inspection and sampling. Preparation of labeling components/outserts inspection reports; quarantine and release labels and maintaining incoming components log and corresponding inventory cards. Issuance of labeling components/outserts according to packaging order and regular monitoring and auditing of label room. Fill out the QA final labeled product inspection report, final line clearance which includes labeling and packaging reconciliation paperwork.
- Compliance of Warehouse area in terms of Isolation of Quarantine, Released, In-Process, Finished Product, Packaged Product, Returned Goods, and Rejected areas.
- Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record Monitor facility and product environmental operating conditions
Additional Responsibilities:
- Operate, maintain and calibrate Hardness tester, Friabilator, Weight Variation system, weighing scales and balances, label counting machine, and Kirby Lester tablet counters according to established schedules and maintain detailed calibration records
- Collection of samples to reassay bulk finished product before expiration
- Work in a Contained Manufacturing area/facility following all precautions and procedures
- Visual inspection and preparation of report of all products for APR
- Other duties as assigned by management.
Education:
- High School or GED - Required
Experience:
- 1 year or more in 1 year in QA or related field
Specialized Knowledge:
- Good basic math knowledge and excellent attention to details. Records observations for improving processes.
Additional Requirement: This position requires successful completion of an OSHA-compliant Respirator Fit Test.
The hourly base salary for this position ranges from $19.50 to $23.50 per hour. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities.
Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com . Requests will be handled confidentially and in accordance with applicable laws.
Description:
The QA Inspector monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run.
Essential Functions:
- Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. Preparation of samples for chemical and microbiological (where required) analysis and delivering them to the QC lab. Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance to specifications. Maintaining detailed records of sampling, inspections and testing activities. Assigning and verification of expiry date and retest date for all the GMP raw materials through vendor COA and in-house COA. Collection of packaged product samples for annual stability.
- Perform room, equipment, and packaging line checks (where applicable) prior to each stage of manufacturing following detailed written procedures. Conduct in process testing per manufacturing and packaging batch record instructions. Prepare controlled / uncontrolled / packaged finished product samples for QC lab and QA retains, following detailed documentation procedures. Maintenance of standard weights required to perform daily verification of balances.
- Labeling component receipt, visual examination, counting, preliminary inspection and sampling. Preparation of labeling components/outserts inspection reports; quarantine and release labels and maintaining incoming components log and corresponding inventory cards. Issuance of labeling components/outserts according to packaging order and regular monitoring and auditing of label room. Fill out the QA final labeled product inspection report, final line clearance which includes labeling and packaging reconciliation paperwork.
- Compliance of Warehouse area in terms of Isolation of Quarantine, Released, In-Process, Finished Product, Packaged Product, Returned Goods, and Rejected areas.
- Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record Monitor facility and product environmental operating conditions
Additional Responsibilities:
- Operate, maintain and calibrate Hardness tester, Friabilator, Weight Variation system, weighing scales and balances, label counting machine, and Kirby Lester tablet counters according to established schedules and maintain detailed calibration records
- Collection of samples to reassay bulk finished product before expiration
- Work in a Contained Manufacturing area/facility following all precautions and procedures
- Visual inspection and preparation of report of all products for APR
- Other duties as assigned by management.
Education:
- High School or GED - Required
Experience:
- 1 year or more in 1 year in QA or related field
Specialized Knowledge:
- Good basic math knowledge and excellent attention to details. Records observations for improving processes.
Additional Requirement: This position requires successful completion of an OSHA-compliant Respirator Fit Test.
The hourly base salary for this position ranges from $19.50 to $23.50 per hour. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities.
Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com . Requests will be handled confidentially and in accordance with applicable laws.
See All 104+ 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
- Biotechnology & Pharmaceuticals
- Consumer Goods
- Food & Beverage
- Science & Research
- Technology & Software
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 Curia, NTT DATA, and 1199 SEIU, based on current listings on Migrate Mate as of August 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, Brooklyn, and Rochester. 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 30% of qa manager openings tied to New York are remote or hybrid as of August 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 104+ QA Manager Jobs in New York
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