Home › Companies › Hcfa Fa Us2 Oraclecloud Com CX › QA Auditing Reviewer
QA Auditing Reviewer
Hcfa Fa Us2 Oraclecloud Com CX · Piscataway, NJ, United States; Piscataway, Piscataway, NJ, US · Active · Oracle Recruiting Cloud / Fusion HCM
Job facts
| Field | Value |
|---|---|
| Company | Hcfa Fa Us2 Oraclecloud Com CX |
| Title | QA Auditing Reviewer |
| Normalized title | - |
| Department / team | Quality Assurance |
| Location | Piscataway, NJ, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-06-18 / 2026-06-19 |
| Changed / last seen | 2026-06-19 / 2026-06-19 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Hcfa Fa Us2 Oraclecloud Com CX. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Piscataway. | Open |
| Department jobs | Active postings in Quality Assurance. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Hcfa Fa Us2 Oraclecloud Com CX |
| Source | 883d3ac1-899e-4648-b63e-68f77e57060e |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
Description
Description
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 needed
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.
Company
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 [email protected] . Requests will be handled confidentially and in accordance with applicable laws.
Full job record
| Job ID | c3d282660ddb7a87f0175c8a5a47fcd282a807a3 |
| Org ID | 78a2aa0e-dc9e-4112-a79f-9ca9a23a5ca6 |
| Source ID | 883d3ac1-899e-4648-b63e-68f77e57060e |
| Board ID | 883d3ac1-899e-4648-b63e-68f77e57060e |
| Provider | oracle_hcm |
| Provider Job Key | 8204 |
| Title | QA Auditing Reviewer |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Piscataway, NJ, United States; Piscataway, Piscataway, NJ, US |
| Department | Quality Assurance |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | NJ |
| City | Piscataway |
| Salary Raw | Description 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 needed 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. Company 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 [email protected] . Requests will be handled confidentially and in accordance with applicable laws. |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealCareers/job/8204 |
| Apply URL | https://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealCareers/job/8204 |
| First Seen At | 2026-06-19 11:28:04Z |
| Last Seen At | 2026-06-19 11:28:04Z |
| Last Checked At | 2026-06-19 11:28:04Z |
| Last Changed At | 2026-06-19 11:28:04Z |
| Inactive At | — |
| Source Posted At | 2026-06-18 17:20:05Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=hcfa.fa.us2.oraclecloud.com|CX/date=2026-06-19/2026-06-19T11-27-57-365Z-74aeef7afba9a8e1c7651a603308df207699274489bfc8defc12931aaa336bf2.json |
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