Pharmaceutical Manufacturing Operator (cGMP)
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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
Update and follow Standard Operating Procedures (SOPs)
Education & Experience
Required:
High School Diploma or equivalent
Preferred:
- Previous manufacturing experience
- Experience working in a GMP-regulated industry (pharmaceutical, biotech, or medical device)