
1st Shift Granulation Operator
PROMAN Staffing USA, Piscataway, NJ, United States
1st Shift Granulation Operator
PROMAN Staffing
Piscataway, NJ, United States of America
1m ago
Role Overview: Responsible for the preparation and processing of raw materials into granulated forms, ensuring equipment integrity and strict adherence to batch records.
Key Responsibilities:
Production Execution: Operate granulation equipment as per Standard Operating Procedures (SOPs) for optimization, validation, and commercial batches.
Documentation: Accurately complete Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and equipment logbooks.
Maintenance & Calibration: Perform daily verification and monthly calibrations of weighing balances; monitor and log area environmental conditions.
Sanitation & Compliance: Clean equipment accessories and process areas according to SOPs; strictly follow facility gowning procedures.
Inventory & Integrity: Manage the inventory, retrieval, and integrity checks of FBP/FBD bags, sieves, and screens.
Technical Support: Participate in Equipment Qualification (IQ/OQ/PQ) and perform other duties as assigned by the Reporting Manager.
Qualifications:
Education: Preferably a Science background.
Experience: 35 years of pharmaceutical manufacturing experience is essential.
PROMAN Staffing
Piscataway, NJ, United States of America
1m ago
Role Overview: Responsible for the preparation and processing of raw materials into granulated forms, ensuring equipment integrity and strict adherence to batch records.
Key Responsibilities:
Production Execution: Operate granulation equipment as per Standard Operating Procedures (SOPs) for optimization, validation, and commercial batches.
Documentation: Accurately complete Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and equipment logbooks.
Maintenance & Calibration: Perform daily verification and monthly calibrations of weighing balances; monitor and log area environmental conditions.
Sanitation & Compliance: Clean equipment accessories and process areas according to SOPs; strictly follow facility gowning procedures.
Inventory & Integrity: Manage the inventory, retrieval, and integrity checks of FBP/FBD bags, sieves, and screens.
Technical Support: Participate in Equipment Qualification (IQ/OQ/PQ) and perform other duties as assigned by the Reporting Manager.
Qualifications:
Education: Preferably a Science background.
Experience: 35 years of pharmaceutical manufacturing experience is essential.