Supervisor, Quality Assurance
Amneal Pharmaceuticals
August 14, 2026
On-site
Piscataway, NJ
Operations
The Supervisor, Quality Assurance schedules and coordinates daily priorities for incoming raw materials and labeling components, in-process testing, finished product sampling, in-process labeling and packaging operations, sampling and inspection activities on all work shifts.
Essential Functions:
- Schedule and coordinate daily priorities for sampling and inspection activities for incoming raw materials, in-process material, finished product, and in-process packaging/labeling operations.
- Train, supervise, and evaluate QA inspectors, QA specialists, and QA auditors to ensure compliance with SOPs/cGMP.
- Monitor QA throughout in-process/packaging operations to ensure compliance with cGMP/SOPs.
- Assist with development/revision of SOPs; execute validation/qualification studies; perform investigations and other assignments as required.
- Manage Change Controls, Deviations, CAPA using effective quality management tools.
- Handle customer complaints (retrieve samples, perform applicable tests, prepare reports, submit by due date).
- Ensure batch records are audited per manufacturing/packaging/shipping requirements (when required).
- Conduct internal audits for compliance with SOP, cGMP & FDA requirements.
Additional Responsibilities:
- Initiate, investigate, and complete CAPA for QA unplanned deviations under guidance of QA Manager.
- Write/review/revise SOPs as directed by QA Manager/Director.
- Plan, monitor, and supervise cross-training of QA inspectors.
- Monitor absences and prepare Kronos/HR requestions/data change forms for shift personnel (when required).
- Review QA inspector performance in the shift as directed by HR.
Qualifications:
- BS/BA: 1+ year pharmaceutical/manufacturing experience; 1+ year supervisory/lead role.
- AS/AA: 5+ years pharmaceutical/manufacturing experience; 2+ years supervisory/lead role.
- High school/GED: 3+ years pharmaceutical/manufacturing experience; 5+ years supervisory/lead role.
Required Skills/Knowledge:
- Knowledge of cGMPs.
Compensation:
- Annual salary: $90,000–$105,000; plus possible short-term incentive/bonus within first 12 months.
Essential Functions:
- Schedule and coordinate daily priorities for sampling and inspection activities for incoming raw materials, in-process material, finished product, and in-process packaging/labeling operations.
- Train, supervise, and evaluate QA inspectors, QA specialists, and QA auditors to ensure compliance with SOPs/cGMP.
- Monitor QA throughout in-process/packaging operations to ensure compliance with cGMP/SOPs.
- Assist with development/revision of SOPs; execute validation/qualification studies; perform investigations and other assignments as required.
- Manage Change Controls, Deviations, CAPA using effective quality management tools.
- Handle customer complaints (retrieve samples, perform applicable tests, prepare reports, submit by due date).
- Ensure batch records are audited per manufacturing/packaging/shipping requirements (when required).
- Conduct internal audits for compliance with SOP, cGMP & FDA requirements.
Additional Responsibilities:
- Initiate, investigate, and complete CAPA for QA unplanned deviations under guidance of QA Manager.
- Write/review/revise SOPs as directed by QA Manager/Director.
- Plan, monitor, and supervise cross-training of QA inspectors.
- Monitor absences and prepare Kronos/HR requestions/data change forms for shift personnel (when required).
- Review QA inspector performance in the shift as directed by HR.
Qualifications:
- BS/BA: 1+ year pharmaceutical/manufacturing experience; 1+ year supervisory/lead role.
- AS/AA: 5+ years pharmaceutical/manufacturing experience; 2+ years supervisory/lead role.
- High school/GED: 3+ years pharmaceutical/manufacturing experience; 5+ years supervisory/lead role.
Required Skills/Knowledge:
- Knowledge of cGMPs.
Compensation:
- Annual salary: $90,000–$105,000; plus possible short-term incentive/bonus within first 12 months.