QC Analyst, First Shift

Agilent Technologies•Frederick, MD

6d•Onsite

About The Position

The QC Analyst conducts routine and non-routine analyses of in-process samples, products, and finished products according to standard operating procedures. Testing includes UV-Vis, HPLC, LC-MS, density, IC solution preparation, and basic sample preparation. The role performs biochemical and/or chemical analyses to assess products and in-process items, including stability, and compiles data documenting test procedures and assays. The analyst calibrates and maintains laboratory equipment, reviews data for compliance with specifications, reports abnormalities, and may help prepare investigations, summaries, and reports. The role also revises and updates standard operating procedures as needed and may undertake special projects involving analytical and instrument problem-solving. This is a full-time, on-site position with a schedule of 8:00 AM–4:30 PM.

Requirements

Bachelor's or master's degree.
Knowledge of FDA requirements.
At least 2 years of relevant experience.

Nice To Haves

Post-graduate education, certification, and/or license may be required.

Responsibilities

Conduct routine and non-routine in-process testing according to standard operating procedures.
Perform biochemical and/or chemical analyses of products, in-process items, and finished products to assess stability.
Perform testing that includes UV-Vis, HPLC, LC-MS, density, IC solution preparation, and basic sample preparation.
Compile data for documentation of test procedures, including biochemical and chemical assays.
Calibrate and maintain laboratory equipment.
Participate in preparing investigations, summaries, and reports when needed.
Review data for compliance with specifications and report abnormalities.
Revise and update standard operating procedures as needed.
Perform special projects involving analytical and instrument problem-solving as needed.