Pharmaceutical Manufacturing Operator (cGMP)

Null Sto; Saint Petersburg (FL); On-site; USD 35,000 - 50,000; Full time

Job summary

A pharmaceutical company is seeking a Manufacturing Operator to support its production operations in Florida. This role involves ensuring high-quality softgel manufacturing, conducting quality inspections, and maintaining compliance with safety standards in a GMP-regulated environment. Ideal candidates will have a high school diploma and previous manufacturing experience is preferred. The position focuses on operational excellence and offers the opportunity to work in a clean and structured setting.

Qualifications

• Required: High School Diploma or equivalent.
• Preferred: Previous manufacturing experience, experience in a GMP-regulated industry.

Responsibilities

• Perform quality inspections to ensure product standards.
• Complete manufacturing documentation as per SOPs.
• Operate equipment for softgel production.
• Package softgels and maintain work area cleanliness.
• Handle waste in compliance with policies.

Skills

Quality inspections

Equipment operation

Attention to detail

Documentation adherence

Education

High School Diploma or equivalent

Tools

Softgel washers

Counting machines

Scales

Printing machines

Job description

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)