Pharma Manufacturing & Packaging Batch Lead

Amneal Pharmaceuticals LLC; Piscataway Township (NJ); On-site; USD 90,000 - 130,000; Full time

Job summary

Amneal Pharmaceuticals LLC in Piscataway, NJ, is seeking a Group Leader to oversee the manufacturing process of batches using state-of-the-art processing systems, including recipe-controlled HMI controls.

You will verify components, initiate batch records, ensure labels and documentation accuracy, and maintain compliance with cGMP in a fast-paced pharmaceutical environment. This role requires 3+ years of manufacturing experience in pharma or medical devices and a high school diploma or GED.

Qualifications

• High School diploma or GED is required.
• 3+ years of manufacturing experience in the pharmaceutical or medical device industry.

Responsibilities

• Verify all product and packaging/manufacturing components prior to operation and entry into the packaging room; confirm against batch records, work orders and packaging records; ensure accurate data entry and complete documentation for each batch.
• Initiate batch records per production schedule; verify staging status; print and inspect shipper labels for accuracy; ensure 100% label reconciliation and submit reviewed documentation to Quality Assurance.
• Adhere to the manufacturing schedule based on the shipping forecast; identify proper status of components in manufacturing/packaging rooms; dispose of rejected materials per procedures.
• Verify calibration status of all equipment before use; perform setup, operation and cleaning per cGMP; complete ROSS transactions and schedule personnel for efficient processing.
• Comply with Amneal Packaging CAPAs and SOPs; wear safety gear and follow dress code.
• Maintain clean, organized, and compliant manufacturing/packaging rooms to prevent mix-ups and cross-contamination.
• Other duties as assigned.

Education

High School diploma or GED

Job description

Amneal Pharmaceuticals LLC in Piscataway, NJ, is seeking a Group Leader to oversee the manufacturing process of batches using state-of-the-art processing systems, including recipe-controlled HMI controls.

You will verify components, initiate batch records, ensure labels and documentation accuracy, and maintain compliance with cGMP in a fast-paced pharmaceutical environment. This role requires 3+ years of manufacturing experience in pharma or medical devices and a high school diploma or GED.