QC Analyst, First Shift

Agilent Technologies•Frederick, CO

8d•$34 - $53•Onsite

About The Position

The QC Analyst conducts routine and non-routine in-process testing 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 of products, in-process items, and finished products to ensure stability and compliance with established procedures. The analyst compiles data documenting test procedures, which may include biochemical and chemical assays; calibrates and maintains laboratory equipment; participates in preparing investigations, summaries, and reports; reviews data for compliance with specifications and reports abnormalities; revises and updates standard operating procedures as needed; and may take on special projects involving analytical and instrument problem-solving. This is a full-time, on-site position with a schedule of 8:00 AM to 4:30 PM. Travel is not required.

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 ensure stability.
Compile data documenting test procedures, potentially including biochemical and chemical assays.
Calibrate and maintain laboratory equipment.
Participate in preparing investigations, summaries, and reports as needed.
Review data for compliance with specifications and report abnormalities.
Revise and update standard operating procedures as needed.
May perform special projects involving analytical and instrument problem-solving.