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Chemist
Tega Cay, SC
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ClearBridge Executive Search

QC Chemist(2nd Shift)

Job Description

QC Chemist(2nd Shift) Job Description QC Chemist (2nd Shift) \n
Job Type:
Full-Time \n \n Job Description \n 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. \n 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. \n \n Key Responsibilities \n \n Perform release, stability, and special request testing of raw materials and finished products.\n Conduct analytical testing according to Standard Operating Procedures (SOPs), internal methods, and compendial methods.\n Operate and troubleshoot laboratory instruments, including HPLC, GC, FTIR, UV/Vis, and other analytical equipment.\n Perform testing accurately and independently while meeting established deadlines.\n Maintain laboratory equipment and ensure proper calibration and maintenance.\n Assist with investigations involving Out-of-Specification (OOS) results.\n Maintain accurate laboratory records, test results, and documentation.\n Follow cGMP, FDA, USP, and applicable
ISO 17025
testing requirements.\n Support laboratory improvements and assist with training new laboratory personnel.\n Collaborate with Quality Control and other departments to resolve testing issues.\n Maintain a clean, organized, and safe laboratory environment.\n\n \n Qualifications \n \n Bachelor's degree in Chemistry required.\n Concentration in Biochemistry, Inorganic Chemistry, Physical Chemistry, or Polymer Chemistry preferred.\n 1+ years of laboratory experience in a cGMP environment preferred.\n Experience operating analytical laboratory equipment, particularly HPLC and/or GC, preferred.\n Knowledge of laboratory testing procedures, analytical methods, and quality standards.\n Familiarity with FDA, USP, and laboratory documentation requirements.\n Strong analytical, organizational, and problem-solving skills.\n Excellent attention to detail and ability to manage multiple testing priorities.\n Strong communication and teamwork skills.\n Ability to work independently in a fast-paced laboratory environment.\n\n \n
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