New · posted Oct 15
Amneal Pharmaceuticals · Pharmaceuticals
Quality Assurance Inspector II - 2nd Shift
- Brookhaven, NY
- On-site
- Full-time
- Associate & Specialist
Open until filled
The role
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.
What you need
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.
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.
What you'll do
- 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.
- 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.
Pay and benefits
$43,680 – $56,160 a year
Employer provided$21.00 – $27.00 an hour · yearly at 2,080 hours (40 a week)
How this comparesHealth and insurance benefits
401(k) matching contribution
Employee well-being programs
Where you'll work
Brookhaven, NYOn-siteOpen in Maps (opens in a new tab)
More jobs in Brookhaven, NYJob intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 36% below the US median for Quality Assurance roles at this level.
This roleEmployer provided
Associate & Specialist roles in New York15 roles publishing pay
Associate & Specialist roles in the US157 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $43,680 | — | $56,160 |
| New York (middle half) | $61,250 | $81,000 | $86,000 |
| All US (middle half) | $59,000 | $78,500 | $94,000 |
This role: Amneal Pharmaceuticals's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Amneal's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 16 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs7
- Lab testing and methods5
- GMP and compliance2
- Investigations and CAPA1
- Regulatory submissions1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Amneal on Regulatory Jobs
- 14
- Open roles
- 10
- Distinct roles
- 2
- Locations
By discipline
- Quality14 100%
By level
- Senior & Principal7 50%
- Associate & Specialist4 29%
- Manager2 14%
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Quality Assurance Inspector II - 2nd Shift at Amneal
Open until filled. $44K–$56K a year, employer provided.