Compounder Level 1 — 2nd Shift (Pharma)

Pai-Pharma-1; Conestee (SC); On-site; USD 30,000 - 39,000; Full time

Job summary

PAI Pharma in Greenville, SC is seeking a Compounder Level 1 for the 2nd shift to support the formulation of liquid pharmaceutical products in compliance with FDA cGMP. You will prepare materials, read batch records, mix ingredients, and ensure cleanliness of the facility.

You will document process information in batch records, follow SOPs, and participate in daily manufacturing activities. This is a full-time role requiring attention to detail and adherence to safety and quality standards.

Qualifications

• Read batch records and follow written instructions precisely.
• Basic math and measurement skills required for dosing.
• Record process data in batch records/logbooks.

Responsibilities

• Prepare materials and equipment for batch liquid formulation.
• Mix ingredients as directed in batch records.
• Maintain cleanliness of facilities and equipment.
• Read batch records and ask questions to ensure understanding.
• Prepare tanks and equipment for batch production.
• Perform mixing operations following instructions.
• Record all process information accurately.
• Clean equipment and store properly.
• Perform housekeeping per SOP and safety procedures.
• Notify management of discrepancies or manufacturing problems.
• Comply with nicotine-free campus and safety policies.

Skills

Read instructions

Write simple notes

Basic math

Data recording

Troubleshooting

Safety awareness

Education

High school diploma or equivalent

6 months related experience or training

Equivalent education/experience

Job description

PAI Pharma in Greenville, SC is seeking a Compounder Level 1 for the 2nd shift to support the formulation of liquid pharmaceutical products in compliance with FDA cGMP. You will prepare materials, read batch records, mix ingredients, and ensure cleanliness of the facility.

You will document process information in batch records, follow SOPs, and participate in daily manufacturing activities. This is a full-time role requiring attention to detail and adherence to safety and quality standards.