Evening QC Chemist (cGMP Lab)

Employee Relations Associates, Inc.; Lancaster (SC); On-site; USD 52,000 - 68,000; Full time

Benefits offered by this job

TalentBridge benefits program

Job summary

Employee Relations Associates, Inc. in Lancaster, SC seeks a QC Chemist to support the quality laboratory with testing of finished products and raw materials.

The role requires learning instrumentation theory and troubleshooting within a safe work environment while managing time to complete testing. The QC Chemist will operate and learn instrumentation such as HPLC, GC, FTIR, and UV/Vis, train new staff, and stay current with USP, FDA guidelines and ISO 17025 to ensure compliant testing and

Qualifications

• Bachelor's degree in Chemistry required; biochemistry, inorganic, physical or polymer chemistry preferred.
• 1+ years of lab experience in a cGMP environment preferred.
• Experience with GC and/or LC instrumentation preferred.
• Strong interpersonal and teamwork skills required.

Responsibilities

• Perform Release, Stability and Special Request testing using SOPs.
• Independently execute in-house methods with minimal assistance.
• Assist with training and document training per SOPs.
• Maintain calibration and proper operation of lab instruments.
• Stay current with USP, FDA publications and ISO 17025.
• Communicate effectively across departments.
• Attend work regularly and maintain attention to detail.

Skills

Time management

Learning mindset

Instrumentation theory

Team collaboration

Safety mindset

Education

Bachelor's degree in Chemistry

Tools

GC

LC

HPLC

FTIR

UV/Vis

Polarimeter

Dissolution

Disintegration

Job description

Employee Relations Associates, Inc. in Lancaster, SC seeks a QC Chemist to support the quality laboratory with testing of finished products and raw materials.

The role requires learning instrumentation theory and troubleshooting within a safe work environment while managing time to complete testing. The QC Chemist will operate and learn instrumentation such as HPLC, GC, FTIR, and UV/Vis, train new staff, and stay current with USP, FDA guidelines and ISO 17025 to ensure compliant testing and