Quality Control Chemist I - HPLC/GC Analysis

PAI Pharma; Greenville (SC); On-site; USD 60,000 - 90,000; Full time

Job summary

PAI Pharma in Greenville, SC is seeking a Chemist I, II, or III to join the Quality Control team. The role focuses on analyzing drug substances, products, and stability samples using USP/NF methods to ensure compliance and product quality.

Responsibilities include conducting HPLC/GC or wet chemistry analyses, documenting results per SOPs, supporting manufacturing schedules, training laboratory staff, and assisting in investigations and CAPAs as needed.

Qualifications

• This position requires a Bachelor’s degree in chemistry, biochemistry, biology or related science.
• Experience with GMP and laboratory software is preferred.
• Proficiency with MS Office and chromatographic software is required.

Responsibilities

• Analyze drug substances, products, and stability samples per SOPs and USP methods.
• Perform HPLC/GC analyses and related sample prep as instructed by QC Supervisor.
• Document all analyses accurately and support manufacturing schedule.
• Assist in training lab personnel and reviewing documentation.
• Support investigations (OOS) and CAPAs as needed.

Skills

HPLC/GC methods

Analytical chemistry

GMP experience

Documentation & SOPs

OpenLab/LIMS experience

Education

Bachelors degree in chemistry or related science

MS/PhD in science (preferred for higher level)

Tools

OpenLab

LIMS

Empower

Job description

PAI Pharma in Greenville, SC is seeking a Chemist I, II, or III to join the Quality Control team. The role focuses on analyzing drug substances, products, and stability samples using USP/NF methods to ensure compliance and product quality.

Responsibilities include conducting HPLC/GC or wet chemistry analyses, documenting results per SOPs, supporting manufacturing schedules, training laboratory staff, and assisting in investigations and CAPAs as needed.