Quality Control Chemist; FDA Regulated

This is a permanent, full-time, salaried position with an amazing nutraceutical manufacturing company! Apply today!

• The Quality Control Chemist I (QCC) reports to Quality Control (QC) Management.
• Perform release, stability and special request testing of finished products and raw materials following Standard Operating Procedures (SOPs), in‑house test methods, and/or compendial methods.
• Train on the operation of the following instrumentation but not limited to:
  Laboratory Balances, High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Automated Titrators, FTIR, UV/Vis Spectrophotometer, Polarimeter, Dissolution and Disintegration Instrumentation. The operation of additional instrumentation and the need to train on new laboratory test methods when required.
• The QCC stays current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control laboratory complies in the areas of analytical applications, release specifications, and documentation practices.
• The QCC assists QC management and/or designee in resolving Out of Specification (OOS) results in the QC Laboratory. Communicate effectively with QC management and with the Out‑of‑Specification/Trend Coordinator when suspect results are generated as well as with the Stability Coordinator when needed.
• The QCC assists in training new laboratory personnel and documents training in accordance with established laboratory SOPs and the company training program.
• The QCC follows Current Good Manufacturing Practice (cGMP) documentation guidelines to record all procedures in a timely fashion.
• Maintain a safe working environment and ensure that all equipment used in the testing procedures is calibrated and properly maintained.
• The QCC competes in specific projects assigned by management and other necessary functions.
• Perform other assigned duties as may be required in meeting company objectives.
• Communicate effectively with other departments within the organization and function within a team environment.
• Regular attendance is required.

0 - 5 years of laboratory experience working in a cGMP environment preferred. Experience preferred with operation of laboratory instrumentation including Gas Chromatography (GC) and/or Liquid Chromatography (LC), troubleshooting, generation and revision of operating procedures and test methods. Effective interpersonal, self‑motivation skills, and the ability to interact with all levels of personnel are required.

A Bachelor of Science (B.S.) or Bachelor of Arts (B.A.) degree in Chemistry