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Pharmaceutical Manufacturing Operator; cGMP

Job in Saint Petersburg, Pinellas County, Florida, 33739, USA
Listing for: Null Sto
Full Time position
Listed on 2026-01-24
Job specializations:
  • Manufacturing / Production
    Manufacturing Production, Pharmaceutical Manufacturing, Operations Engineer, Quality Engineering
Job Description & How to Apply Below
Position: Pharmaceutical Manufacturing Operator (cGMP)

About the Role

Catalent Pharma Solutions is seeking a Manufacturing Operator to support its pharmaceutical production operations in a cGMP-regulated environment
. This role plays a critical part in ensuring high-quality softgel manufacturing, inspection, and packaging while maintaining strict safety and quality standards.

You will work in a clean, safe, and structured manufacturing environment focused on operational excellence, quality compliance, and continuous improvement.

Key Responsibilities
  • Perform quality inspections to identify and remove sub-standard softgels and foreign materials
  • Accurately complete manufacturing and finishing documentation per SOPs and cGMP requirements
  • Operate equipment including softgel washers, counting machines, scales
    , and printing machines (as required)
  • Inspect, clean, stage, and handle tray stacks for inspection and packaging
  • Conduct line clearances between product lots
  • Package softgels in bulk and ensure proper labeling and identification of cartons
  • Transfer sealed cartons to warehouse or staging areas as needed
  • Maintain a clean and organized work area
  • Handle non-hazardous, hazardous, and DEA waste in compliance with policies
  • Immediately report potential quality issues to supervision/QA
  • Support cross-training and assist in other production areas when required
Education & Experience

Required: High School Diploma or equivalent

Preferred: Previous manufacturing experience;
Experience working in a GMP-regulated industry (pharmaceutical, biotech, or medical device)

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