Chemist II: cGMP Analytics, Troubleshooting & Training

International Vitamin Corporation

Anderson (SC)

Hybrid

USD 65,000 - 90,000

Full time

12 days ago

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Job summary

International Vitamin Corporation (IVC) is seeking a Chemist II to perform quantitative and qualitative analyses of raw materials, finished products, and stability samples in a FDA-controlled environment. The role requires cGMP/cGLP familiarity and collaboration with Quality Management for special projects and method development.

The candidate will train others on specific instruments, follow SOPs, and maintain audit-ready lab practices while supporting multiple departments with data

Qualifications

  • 1-3 years’ experience in a cGMP environment.
  • BA or BS Degree in Chemistry or related science.
  • Strong troubleshooting and documentation skills.
  • Ability to train others and supervise as needed.

Responsibilities

  • Performs chemical testing of incoming raw materials, finished product, and stability samples using HPLC, GC, and ICP/ICPMS.
  • Follow cGMPs, cGLPs, Compendia, and SOPs.
  • Maintain lab areas and prepare reagents; clean glassware and equipment.
  • Perform routine equipment maintenance checks and calibrations.
  • Support other departments on special projects as needed.
  • Gather, interpret, and review analytical data.
  • Ensure audit readiness of the lab.
  • Train others on instruments or techniques as needed.
  • Assist in troubleshooting and investigations of out-of-spec results.
  • Contribute to SOP updates.

Skills

cGMP experience
Data analysis
Troubleshooting

Education

BA/BS in Chemistry

Tools

HPLC
GC
ICP/ICPMS

Job description

International Vitamin Corporation (IVC) is seeking a Chemist II to perform quantitative and qualitative analyses of raw materials, finished products, and stability samples in a FDA-controlled environment. The role requires cGMP/cGLP familiarity and collaboration with Quality Management for special projects and method development.

The candidate will train others on specific instruments, follow SOPs, and maintain audit-ready lab practices while supporting multiple departments with data

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