Pharma Compounder – Entry Level (FDA cGMP)

PAI Pharma; Greenville (SC); On-site; USD 42,000 - 54,000; Full time

Job summary

PAI Pharma in Greenville, SC is seeking a Full Time Operator to prepare materials and equipment for liquid formulation in compliance with FDA cGMP requirements. The role involves mixing ingredients, reading batch records, and maintaining a clean, safe production area.

You will follow SOPs, document all process information, and support department housekeeping. The position requires physical ability to handle weights and to work a full 40-hour week, with attention to detail and a willingness to

Qualifications

• Read batch records and follow written instructions precisely.
• Maintain cleanliness and comply with FDA cGMP requirements.
• Ability to stand, lift up to 25–100 pounds as needed.

Responsibilities

• Prepare materials and equipment for liquid formulation per batch records.
• Mix ingredients according to batch instructions to produce liquids.
• Record process information in batch records and logbooks.
• Clean equipment and maintain a tidy work area.
• Comply with SOPs, cGMP, and safety procedures.
• Notify management if discrepancies arise.

Skills

Read and understand instructions

Write simple correspondence

Basic math (units, fractions)

Interpret batch records

Attention to detail

Compliance with SOPs

Education

High school diploma or equivalent + related training

Job description

PAI Pharma in Greenville, SC is seeking a Full Time Operator to prepare materials and equipment for liquid formulation in compliance with FDA cGMP requirements. The role involves mixing ingredients, reading batch records, and maintaining a clean, safe production area.

You will follow SOPs, document all process information, and support department housekeeping. The position requires physical ability to handle weights and to work a full 40-hour week, with attention to detail and a willingness to