GMP Production Technician – IV Packaging

B. Braun US Pharmaceutical Manufacturing LLC

Irvine (CA)

On-site

USD 32,000 - 45,000

Full time

8 days ago

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Job summary

B. Braun Medical, Inc. in Irvine, California is seeking a dedicated Production Operator to support the safe and efficient manufacturing of IV products in an FDA-regulated, cGMP environment.

This onsite role requires attention to quality, timely documentation, and precise operation of production equipment on a 3/4 X 12 shift. You will set up and run equipment, load/unload IV bags, inspect materials, move pallets, document activities, and assist with routine maintenance.

Qualifications

  • High school diploma or GED required.
  • 3+ years in production/manufacturing or equipment operation.
  • Experience in regulated manufacturing environment.
  • Ability to follow detailed instructions and procedures.
  • Basic troubleshooting and problem-solving skills.

Responsibilities

  • Perform production activities in accordance with FDA regulations, cGMP, safety standards, and established procedures.
  • Set up, clean, adjust, and operate production equipment while resolving jams and supporting basic troubleshooting and preventive maintenance activities.
  • Load and unload IV bags, inspect materials as required, and package finished IV bags into cases.
  • Move, reposition, and transfer pallets and production materials safely throughout the assigned work area.
  • Complete required cleaning activities and accurately document work in production logbooks.
  • Follow good documentation practices when entering information in batch records and recording completed activities.
  • Support other product lines or departments as operational needs require.

Skills

Production experience
Regulated environment knowledge
Attention to instructions
Troubleshooting

Education

High school diploma or GED

Job description

B. Braun Medical, Inc. in Irvine, California is seeking a dedicated Production Operator to support the safe and efficient manufacturing of IV products in an FDA-regulated, cGMP environment.

This onsite role requires attention to quality, timely documentation, and precise operation of production equipment on a 3/4 X 12 shift. You will set up and run equipment, load/unload IV bags, inspect materials, move pallets, document activities, and assist with routine maintenance.

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