Quality Control Chemist - cGMP Regulated Lab Expert

EPM Scientific; Lancaster (SC); On-site; USD 70,000 - 85,000; Full time

Job summary

EPM Scientific in Lancaster, SC is seeking a Quality Laboratory Chemist I/II to perform analytical testing in a regulated manufacturing environment. You will support methods, maintain compliance with procedures, and contribute to continuous laboratory improvement efforts.

The ideal candidate will have experience in FDA-regulated, cGMP-compliant labs and be comfortable with data integrity and regulatory expectations. Strong attention to detail is essential.

Qualifications

• Bachelor's degree in Chemistry or related scientific discipline.
• Minimum 2 years of analytical laboratory experience preferred.
• Experience in FDA-regulated and cGMP-compliant environments preferred.
• Experience independently executing analytical methods.
• Commitment to data integrity and GDP principles.

Responsibilities

• Perform routine and non-routine testing of raw materials, in-process samples, stability samples, and finished products.
• Document testing activities and results in accordance with procedures and GDP.
• Review analytical data for accuracy and compliance with specifications.
• Support investigations related to OOS, OOT, and atypical results.
• Train laboratory personnel on testing procedures and instrumentation.
• Collaborate with QA, Manufacturing, Regulatory Affairs, and Technical Operations.

Skills

Analytical thinking

Troubleshooting

Attention to detail

Documentation

Communication

Time management

Education

Bachelor's degree in Chemistry

Tools

GC

Dissolution Testing

Wet Chemistry

Titration Techniques

Empower software

Chromatography data systems

Job description

EPM Scientific in Lancaster, SC is seeking a Quality Laboratory Chemist I/II to perform analytical testing in a regulated manufacturing environment. You will support methods, maintain compliance with procedures, and contribute to continuous laboratory improvement efforts.

The ideal candidate will have experience in FDA-regulated, cGMP-compliant labs and be comfortable with data integrity and regulatory expectations. Strong attention to detail is essential.