QA Auditing Reviewer

Amneal Pharmaceuticals; Newtown (NJ); On-site; USD 30,000 - 44,000; Full time

Job summary

Amneal Pharmaceuticals is seeking a QA Auditing Reviewer to audit production records, determine batch disposition, and execute those decisions in JDE. You will ensure held or rejected batches are properly stored and you will log RFT data and load batch information into the APR database.

You may fill in for in-process QA inspectors when needed, collaborating with QA teams to maintain GMP compliance and accurate documentation across all manufacturing stages.

Qualifications

• High School diploma or GED required; Bachelor's degree preferred.
• 2+ years in Pharmaceutical QA, QC or QM.
• GMP knowledge; familiarity with 21 CFR Parts 210, 211, 820 and ICH guidance.

Responsibilities

• Audit production records and determine batch disposition (Release, Hold, Reject).
• Physically perform batch disposition in JDE for each lot.
• Ensure batches on Hold/Reject are stored in designated limited-access areas.
• Log RFT data per QA processes; load batch data into APR database if required.
• Communicate clearly, both orally and in writing; operate calculators and PCs.
• Perform timely reviews of QA In-Process Data.

Skills

Calibration

Data Entry

Detail Oriented

Facility Inspection

First Article Inspections

Good Manufacturing Practices

Laboratory Information Management "S"

Quality Management Systems

Visual Inspections

Education

High School or GED

Bachelor's Degree in Related Field

Tools

JDE

APR database

Job description

This QA Auditing Reviewer role is responsible for thoroughly auditing production records, determining batch disposition (Release, Hold, Reject), and executing those decisions in systems like JDE while ensuring held or rejected batches are properly controlled and stored. It also logs and loads batch data into required databases, regularly audits QA in‑process data, and may fill in for in‑process QA inspectors when needed.

Essential Functions

• Thoroughly audit all production records (work order #1 and #2 for commercial and exhibit batches) and determine batch disposition (Release, Hold, Reject). Physically perform batch disposition for each lot of product produced, including making the correct entries in JDE.
• Responsible for making sure Batches placed on Hold or Reject status are appropriately stored in their designated limited access areas.
• Log RFT data in accordance with established QA Processes
• Load batch data into the APR database (if required)
• Communicating clearly and concisely, both orally and in writing.
• Operating scientific calculators and personal computers
• Performs timely reviews of QA In-Process Data

Additional Responsibilities

• Must be able to fill in for In-process QA inspectors when circumstances dictate

Qualifications

Education

• High School or GED - Required

Bachelors Degree in Related Field - Preferred

Experience:

2 years or more in Pharmaceutical QA, QC or QM

Specialized Knowledge

• Excellent knowledge of manufacturing processes from Raw Material Receipt through finished goods packaging
• Comprehensive understanding of GMP standards, including 21 CFR Parts 210, 211, 820, and relevant ICH guidance.

The hourly rate for this position ranges from $22.00-$32.00 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months. Amneal ranges reflect the Company’s good faith estimate of what 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, experience, 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 help you enjoy your career alongside life’s many other commitments and opportunities.

Required Skills

• Calibration
• Data Entry
• Detail Oriented
• Facility Inspection
• First Article Inspections
• Good Manufacturing Practices
• Laboratory Information Management Systems
• Quality Management Systems
• Visual Inspections

About Us

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 [e-mail] . Requests will be handled confidentially and in accordance with applicable laws.

Job Info

• Job Identification 8410
• Job Category Quality Assurance
• Posting Date 08/11/2026, 01:54 PM
• Locations 49 Colonial Drive, Piscataway, NJ, 08854, US