Pharma Manufacturing Operator III — Dosage Forms

Amneal Pharmaceuticals LLC; Piscataway Township (NJ); On-site; USD 32,000 - 44,000; Full time

Benefits offered by this job

Bonus opportunity

Healthcare benefits

401(k) matching

Job summary

Amneal is seeking a Production Operator III to execute manufacturing operations for solid oral dosage forms, including granulation, blending, compression, and coating. The role requires 3+ years in pharmaceutical manufacturing and hands‑on experience with batch records and cGMP documentation.

You will plan, prioritize, and run assigned processes to meet production schedules, while accurately recording in-process tests and data.

Qualifications

• 3+ years of experience in pharmaceutical manufacturing, preferably in solid oral dosage manufacturing.
• Hands-on experience in granulation, blending, compression, fluid bed processing, and coating.
• Knowledge of cGMP documentation and batch records.
• Ability to calculate batch records and perform in-process testing.
• Familiarity with Safety Data Sheets (SDS) and site safety procedures.

Responsibilities

• Performs commercial manufacturing operations for solid oral dosage forms per batch records and SOPs.
• Runs processes to meet production schedules; communicates deviations to supervisor.
• Independently perform B-stage reconciliation activities per SOPs and cGMP.
• Plan and prioritize activities to meet deadlines and production targets.
• Analyze process issues and support troubleshooting with clear documentation.
• Conduct in-process testing (LOD, disintegration, bulk density, tablet hardness, thickness, friability, weight).

Skills

Granulation

Blending

Compression

Coating

cGMP knowledge

SOP adherence

Data recording

Education

High School or GED

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Job description

Amneal is seeking a Production Operator III to execute manufacturing operations for solid oral dosage forms, including granulation, blending, compression, and coating. The role requires 3+ years in pharmaceutical manufacturing and hands‑on experience with batch records and cGMP documentation.

You will plan, prioritize, and run assigned processes to meet production schedules, while accurately recording in-process tests and data.