Quality Assurance Inspector Jobs in New York
Quality Assurance Inspector jobs in New York are concentrated in manufacturing, pharmaceuticals, food processing, and aerospace defense, with strong demand at every level from entry-level floor inspector to senior quality engineer. The heaviest hiring is in New York City, Buffalo, and Rochester, where employers like Pfizer, Lockheed Martin, and Corning maintain major production and R&D operations. The most in-demand specialties are pharmaceutical compliance, aerospace parts inspection, and food safety auditing. Find a role that fits below and apply directly.
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Showing 5 of 8+ Quality Assurance Inspector jobs
Description:
To monitor and ensure 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. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run.
Schedule:
2nd Shift 3:30pm - 12:00 AM Monday to Friday
Essential Functions:
- All Functions of QA Inspector I, 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 perfomr 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. Plus the following:
- Review of engineering records (temperature and humidity data calibration and PM records, Pest control records and contractor related functions)
- Review of online batch records in terms of completeness of signatures, entries, and actual reconcilaiton / yields prior to initiation of next processing step
- Verification of functionality of all the equipment and associated controls during the batch run Maintenance of retention sample room and monitoring of temperature and humidity, replacement fo chart records as per schedule, review of log and disposition of samples.
Additional Responsibilities:
- Disposition of rejected material and returned drug products as per SOP
- Performs environmental monitoring in accordance with established schedule (where applicable)
- Perform applicable testing and prepare report for customer complaints
- Other duties that management may from time to time assign.
Education:
- High School or GED - Required
Experience:
- 2 years or more in 2 or more years experience 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 $21.00 to $27.00 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:
To monitor and ensure 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. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run.
Schedule:
2nd Shift 3:30pm - 12:00 AM Monday to Friday
Essential Functions:
- All Functions of QA Inspector I, 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 perfomr 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. Plus the following:
- Review of engineering records (temperature and humidity data calibration and PM records, Pest control records and contractor related functions)
- Review of online batch records in terms of completeness of signatures, entries, and actual reconcilaiton / yields prior to initiation of next processing step
- Verification of functionality of all the equipment and associated controls during the batch run Maintenance of retention sample room and monitoring of temperature and humidity, replacement fo chart records as per schedule, review of log and disposition of samples.
Additional Responsibilities:
- Disposition of rejected material and returned drug products as per SOP
- Performs environmental monitoring in accordance with established schedule (where applicable)
- Perform applicable testing and prepare report for customer complaints
- Other duties that management may from time to time assign.
Education:
- High School or GED - Required
Experience:
- 2 years or more in 2 or more years experience 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 $21.00 to $27.00 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 8 Quality Assurance Inspector Jobs in New York
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Find JobsQuality Assurance Inspector Jobs by City in New York
Where New York roles are concentrated, by current openings.
Quality Assurance Inspector 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
What New York Employers Look For
The qualifications that appear most often in quality assurance inspector jobs across New York.
- High school diploma or associate degree in a technical or manufacturing-related field
- Experience reading and interpreting engineering drawings, blueprints, and specifications
- Familiarity with quality management systems such as ISO 9001 or AS9100
- Proficiency with precision measurement tools including calipers, micrometers, and gauges
- Knowledge of Good Manufacturing Practices relevant to pharmaceutical or food industries
- Strong written documentation skills for recording inspection results and nonconformance reports
Quality Assurance Inspector Jobs in New York: Frequently Asked Questions
How do you become a quality assurance inspector in New York?
Most quality assurance inspector roles in New York require at least a high school diploma plus on-the-job experience, though an associate or bachelor's degree in engineering technology, manufacturing, or a related field significantly improves your chances. New York has no single mandatory state license for general quality inspectors, but pharmaceutical and food sector roles often require documented GMP training and may involve FDA-regulated facilities. Certifications from the American Society for Quality, such as the Certified Quality Inspector credential, are widely recognized by New York employers and can substitute for experience in competitive openings.
Which companies hire quality assurance inspectors in New York?
Employers hiring quality assurance inspectors in New York right now include Amneal Pharmaceuticals, AECOM, and Tiffany &, based on current listings on Migrate Mate as of September 2026. New York's pharmaceutical, defense, and food manufacturing sectors drive consistent year-round demand across the state.
Which New York cities have the most quality assurance inspector jobs?
Hauppauge, Brookhaven, and Albany have the most quality assurance inspector openings in New York. New York City anchors demand through its large pharmaceutical and consumer goods operations, while Buffalo and Rochester draw on deep aerospace and precision manufacturing industries rooted in companies like Moog, Kodak's successor businesses, and regional defense contractors, making upstate New York a consistent source of openings outside the metro.
Are there remote quality assurance inspector jobs in New York?
Yes, but they're rare. Quality assurance inspector work is fundamentally hands-on, requiring physical presence to measure parts, audit production lines, and verify materials. About 0% of quality assurance inspector openings tied to New York are remote or hybrid as of September 2026, and those tend to be documentation-heavy roles such as supplier quality auditing or quality management system coordination rather than floor inspection positions.
How can I get hired as a quality assurance inspector in New York with little or no experience?
The most realistic entry path is a production technician or manufacturing associate role at a large New York facility, which regularly moves employees into quality functions after several months. Employers like Pfizer's upstate New York plants, Lockheed Martin in Owego, and major food processors in the Hudson Valley run structured on-the-job training for associates without inspection backgrounds. Completing an American Society for Quality Certified Quality Inspector exam preparation course while working on the floor demonstrates seriousness and gives candidates a measurable edge when internal QA openings are posted.
Where can I find and apply to quality assurance inspector jobs in New York?
You can find and apply to quality assurance inspector jobs in New York on Migrate Mate, which lists current openings across the state. Search the listings, find roles that match your background and location, and apply directly to the ones that fit.
See All 8 Quality Assurance Inspector Jobs in New York
Find roles in New York that match your experience and apply in just a few clicks.
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