Quality Assurance Analyst Jobs in New Jersey
Quality Assurance Analyst jobs in New Jersey are among the most active in the Mid-Atlantic region, with strong demand from pharmaceutical and life sciences manufacturers, financial services firms, and enterprise technology companies at every level from entry-level tester through senior QA lead. The heaviest hiring concentrates in Newark, Princeton, and the Route 1 corridor, where employers like Johnson & Johnson, Cognizant, and Merck maintain large operations. The most in-demand specialties are automated testing, regulatory compliance QA within pharma, and software quality assurance for fintech platforms. Find a role that fits below and apply directly.
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Showing 5 of 91+ Quality Assurance Analyst 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.
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 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.
- 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 reconciliation / 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.
-
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.
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 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.
- 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 reconciliation / 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.
-
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 91 Quality Assurance Analyst Jobs in New Jersey
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Find JobsQuality Assurance Analyst Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Quality Assurance Analyst Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Medical Devices
- Biotechnology & Pharmaceuticals
- Retail
- Insurance
- Science & Research
What New Jersey Employers Look For
The qualifications that appear most often in quality assurance analyst jobs across New Jersey.
- Bachelor's degree in computer science, engineering, or a related technical field required
- Proficiency with test automation tools such as Selenium, JIRA, or TestNG
- Experience writing and executing manual and automated test cases and scripts
- Familiarity with FDA 21 CFR Part 11 or pharmaceutical validation regulations preferred
- Strong analytical and problem-solving skills with attention to documentation accuracy
- Experience working within Agile or Scrum development environments and sprint cycles
Quality Assurance Analyst Jobs in New Jersey: Frequently Asked Questions
How do you become a quality assurance analyst in New Jersey?
Most quality assurance analyst roles in New Jersey require a bachelor's degree in computer science, information technology, engineering, or a related field. New Jersey does not issue a state license for this role, but employers in the state's pharmaceutical and life sciences sector often require familiarity with FDA validation standards and Good Manufacturing Practice guidelines. Earning a recognized certification such as ISTQB Foundation Level strengthens a candidate's profile considerably in New Jersey's competitive market.
How much do quality assurance analysts make in New Jersey?
Quality assurance analysts in New Jersey earn a median of about $119,470 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $70,150 for the lowest 10% to over $168,680 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire quality assurance analysts in New Jersey?
Employers hiring quality assurance analysts in New Jersey right now include SGS, MICRO, and Wiz International, based on current listings on Migrate Mate as of November 2026. New Jersey's dense concentration of pharmaceutical headquarters and financial technology firms means hiring is distributed across both large enterprise employers and mid-size specialty contractors throughout the state.
Which New Jersey cities have the most quality assurance analyst jobs?
Princeton, Somerset, and Jersey City have the most quality assurance analyst openings in New Jersey. Newark anchors demand through its financial services and technology sectors, the Princeton and Route 1 corridor draws hiring from pharmaceutical and biotech headquarters, and Jersey City benefits from its proximity to New York City financial institutions that maintain significant New Jersey operations.
Are there remote quality assurance analyst jobs in New Jersey?
Yes, and more than most fields. About 39% of quality assurance analyst openings tied to New Jersey are remote or hybrid as of November 2026, reflecting how naturally suited the role is to distributed work. Software QA, test automation, and documentation-heavy compliance roles are the most likely to be offered fully remote, while hands-on validation roles in pharmaceutical manufacturing typically require an on-site presence.
How can I get hired as a quality assurance analyst in New Jersey with little or no experience?
The most realistic entry path is starting as a junior QA tester or test analyst at a New Jersey technology services firm or staffing contractor, where structured onboarding is common for candidates without prior QA titles. Large employers such as Cognizant and Infosys, both with New Jersey delivery centers, run associate programs that bring in candidates from adjacent roles like business analyst, data entry, or technical support. Building an ISTQB Foundation certification and a portfolio of personal or academic test cases gives candidates a clear edge when applying to these programs.
Where can I find and apply to quality assurance analyst jobs in New Jersey?
You can find and apply to quality assurance analyst jobs in New Jersey on Migrate Mate, which lists current openings from employers actively hiring in the state. Find roles that fit your experience and specialization and apply directly to the ones that match.
See All 91 Quality Assurance Analyst Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
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