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QC Chemist(2nd Shift)

ClearBridge Executive Search
Rock, SC Full Time
POSTED ON 11/12/2026
AVAILABLE BEFORE 12/11/2026

QC Chemist (2nd Shift)

Job Type: Full-Time


Job Description

We are seeking a detail-oriented QC Chemist to support daily laboratory testing and quality control activities. The ideal candidate will have experience in analytical chemistry, laboratory instrumentation, and testing within a cGMP-regulated environment.

This position is responsible for performing raw material and finished product testing, maintaining accurate laboratory documentation, and ensuring compliance with established quality and safety standards.


Key Responsibilities

  • Perform release, stability, and special request testing of raw materials and finished products.
  • Conduct analytical testing according to Standard Operating Procedures (SOPs), internal methods, and compendial methods.
  • Operate and troubleshoot laboratory instruments, including HPLC, GC, FTIR, UV/Vis, and other analytical equipment.
  • Perform testing accurately and independently while meeting established deadlines.
  • Maintain laboratory equipment and ensure proper calibration and maintenance.
  • Assist with investigations involving Out-of-Specification (OOS) results.
  • Maintain accurate laboratory records, test results, and documentation.
  • Follow cGMP, FDA, USP, and applicable ISO 17025 testing requirements.
  • Support laboratory improvements and assist with training new laboratory personnel.
  • Collaborate with Quality Control and other departments to resolve testing issues.
  • Maintain a clean, organized, and safe laboratory environment.


Qualifications

  • Bachelor's degree in Chemistry required.
  • Concentration in Biochemistry, Inorganic Chemistry, Physical Chemistry, or Polymer Chemistry preferred.
  • 1 years of laboratory experience in a cGMP environment preferred.
  • Experience operating analytical laboratory equipment, particularly HPLC and/or GC, preferred.
  • Knowledge of laboratory testing procedures, analytical methods, and quality standards.
  • Familiarity with FDA, USP, and laboratory documentation requirements.
  • Strong analytical, organizational, and problem-solving skills.
  • Excellent attention to detail and ability to manage multiple testing priorities.
  • Strong communication and teamwork skills.
  • Ability to work independently in a fast-paced laboratory environment.


Salary : $70,000 - $80,000

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