Quality Control Chemist — Analytical Testing & GMP

Kelly; Lynchburg (VA); On-site; USD 60,000 - 85,000; Full time

Benefits offered by this job

Medical benefits

Paid holidays

Transit benefit

Job summary

Kelly is seeking a Chemist in Lynchburg, VA to safeguard quality across raw materials, in-process samples, finished products, and stability testing. The role emphasizes analytical testing, documentation, and regulatory compliance in a GMP environment.

Responsibilities include applying HPLC, GC, UV-Vis, TOC, Karl Fischer, and titration methods, while supporting new product development and stability studies. Strong record-keeping and adherence to SOPs are essential.

Qualifications

• Bachelor's degree in Chemistry and GMP experience required.
• Experience with analytical instrumentation and laboratory testing.
• Preferred: Empower, Shimadzu UV-Vis and LabSolutions software.

Responsibilities

• Perform chemical and analytical testing of raw materials, in-process materials, finished products, and stability samples.
• Conduct testing using HPLC, GC, UV-Vis, TOC, Karl Fischer, and titration techniques, using MasterControl for quality and documentation.
• Support new product development and stability studies, including analytical method activities; analyze, document, and report results per specifications.
• Maintain accurate laboratory records and ensure compliance with cGMP, SOPs, and regulatory requirements.
• Support analytical methods related to manufacturing systems and process improvements; communicate issues and assist with investigations.
• Maintain laboratory equipment and ensure testing is performed per validated procedures.

Education

Bachelor's degree in Chemistry

Tools

HPLC

GC

UV-Vis

TOC

Karl Fischer

Titration

Empower

Shimadzu UV-Vis

LabSolutions

Job description

Kelly is seeking a Chemist in Lynchburg, VA to safeguard quality across raw materials, in-process samples, finished products, and stability testing. The role emphasizes analytical testing, documentation, and regulatory compliance in a GMP environment.

Responsibilities include applying HPLC, GC, UV-Vis, TOC, Karl Fischer, and titration methods, while supporting new product development and stability studies. Strong record-keeping and adherence to SOPs are essential.