Chemist - Quality Control (Second Shift)
: Job Details :


Chemist - Quality Control (Second Shift)

Commonwealth Sciences

Location: all cities,SC, USA

Date: 2024-11-06T15:31:03Z

Job Description:

Position located in Caskey, South Carolina

Responsibilities of the Chemist - Quality Control (Second Shift)

  • :Conducting testing of finished products and raw materials, including release, stability, and special request analyses, in adherence to Standard Operating Procedures (SOPs), internal testing methods, and compendial guideline
  • s.Training on the use of various laboratory instruments such as FTIR, UV/Vis Spectrophotometer, Polarimeter, Balances, HPLC, GC, Automated Titrators, and Dissolution and Disintegration Equipment. The QCC will also adapt to training needs for new laboratory methods as require
  • d.Staying informed about updates and publications from regulatory bodies such as the USP and FDA to ensure compliance in analytical methods, release criteria, and documentation standards within the Quality Control laborator
  • y.Assisting QC management and designated personnel in addressing Out of Specification (OOS) results, effectively communicating with QC management, the Out-of-Specification/Trend Coordinator regarding suspect results, and the Stability Coordinator as necessar
  • y.Aiding in the training of new laboratory staff and ensuring proper documentation of training in line with established SOPs and the training framewor
  • k.Following Current Good Manufacturing Practice (cGMP) standards to ensure timely and accurate documentation of all procedure
  • s.Upholding a safe working environment and ensuring that all testing equipment is calibrated and properly maintaine
  • d.Completing specific projects and additional tasks as assigned by management to support operational goal
  • s.Engaging in effective communication with other departments and collaborating within a team-oriented atmospher

e.Requirements of the Chemist - Quality Control (Second Shif

  • t):A BS in chemistry, biochemistry, or biology, with 0-5 years of experience in a cGMP sett
  • ing.Familiarity with laboratory instrumentation operation, particularly Gas Chromatography (GC) and/or Liquid Chromatography (LC), along with troubleshooting skills and experience in creating or revising operating procedures and test methods is prefer

red.
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