QA Supervisor: Lead & Train Inspectors, cGMP

Amneal Pharmaceuticals; Piscataway Township (NJ); On-site; USD 85,000 - 120,000; Full time

Job summary

Amneal Pharmaceuticals is seeking a Supervisor, Quality Assurance to lead daily QA priorities for raw materials, labeling components, in-process testing, finished product sampling, and packaging operations. You will supervise QA inspectors, ensure cGMP/SOP compliance, and drive CAPA initiatives across all shifts.

The role requires a Bachelor’s or equivalent, with 1+ year supervisory experience in pharma manufacturing, strong knowledge of cGMP and SOPs, and a proven track record in QA leadership

Qualifications

• Bachelor’s degree with 1+ year pharmaceutical manufacturing supervision.
• Associate degree with 2+ years supervisory manufacturing experience.
• High school diploma with 5+ years pharmaceutical/manufacturing supervision.
• Knowledge of cGMPs and SOPs compliance.

Responsibilities

• Schedules and coordinates daily priorities for QA inspections, sampling, and packaging operations.
• Trains and evaluates QA inspectors, QA Specialists and QA Auditors for SOP and cGMP compliance.
• Monitors QA in-process and packaging operations to ensure cGMP/SOP compliance.
• Develops and revises SOPs; supports validation and qualification studies.
• Handles CAPA processes and corrective actions.
• Reviews and manages batch records, audits SOPs, and conducts internal audits for compliance.

Skills

Leadership

Supervisory experience

Quality Assurance understanding

Education

Bachelor’s Degree (BA/BS)

Associate Degree (AA/AS)

High School Diploma or GED

Job description

Amneal Pharmaceuticals is seeking a Supervisor, Quality Assurance to lead daily QA priorities for raw materials, labeling components, in-process testing, finished product sampling, and packaging operations. You will supervise QA inspectors, ensure cGMP/SOP compliance, and drive CAPA initiatives across all shifts.

The role requires a Bachelor’s or equivalent, with 1+ year supervisory experience in pharma manufacturing, strong knowledge of cGMP and SOPs, and a proven track record in QA leadership