PACKAGING OPERATOR I

LGM Pharma, LLC•Rosenberg, TX

5d•Onsite

About The Position

This role involves operating and maintaining packaging equipment, ensuring product quality, and adhering to strict regulatory standards. The Packaging Operator I is responsible for setting up, operating, and cleaning various pieces of equipment used in the packaging process, including coating machines, spray guns, and dust collectors. They will perform quality checks, maintain accurate documentation, and ensure a clean and safe work environment. This position requires attention to detail, the ability to follow procedures, and physical capability to handle the demands of the role.

Requirements

High school diploma or General Education Degree (GED).
6 months+ years of related experience, or equivalent combination of education and experience.
Able to follow standard operation procedures (GMP’s, SOP’s and Batch Records).
Able to follow directions and communicate information (written and verbal).
Able to use basic math calculations (add, subtract, multiply, and divide); operate a calculator.
Able to disassemble and reassemble equipment.
Good organization skills.
Strong attention to detail.
Able to lift 25 lbs. repeatedly and 50 pounds occasionally throughout the day.
Able to climb ladders and use balance.
Able to stand for long periods of time and frequently walk.
Able to use hands and arms to feel, reach, and move.

Responsibilities

Sets up equipment to include mixing clear coating solution, lubricating 48” and 60” Acella Cota, and equally splitting lots to coat.
Performs clean-up and disassembles pan blades/baffles, spray guns, 48” Acella Cota Cleaning P5-20-004, 60” Acella Cota Cleaning P5-20-005, and dust collectors.
Operates and adjusts equipment to include prime spray guns, coating tablet with clear coating, Peristaltic Pump, air mixer, loader, unloader, exhaust temperature, exhaust temperature, pan speed, spray patterns, atomization, 48” Acella Cota Operation P5-70-001, and 60” Acella Cota Operation P5-70-002.
Performs inspections and verification of products to include properly waxing tablets, reads, understands and follows batch record and completing associated paperwork as needed.
Ensures room has been released by Quality Assurance as indicated on the Equipment Use / Maintenance Cleaning Log. Makes appropriate entries into log.
Works with Supervisors, Leads, and trainers to verify all procedures have been followed.
Performs all duties according to written Standard Operating Procedures (SOP’s) and in compliance with current Good Manufacturing Practices (cGMP’s), 21 CFR Part 111.
Maintains a clean, neat work area, removing trash and sweeping as necessary.
Performs other related duties as required.