QC Analyst, Associate

Agilent Technologies

1d•$29 - $45•Remote

About The Position

Conducts routine and non-routine analysis of raw materials, in-process items, and finished formulations according to standard operating procedures. Performs biochemical and/or chemical analyses to ensure product stability and compliance with specifications. Compiles data for documentation of test procedures, including biochemical and chemical assays, stability program testing, and formulation studies. Calibrates and maintains laboratory equipment, participates in investigations, and prepares summaries and reports. May develop testing methods, revise SOPs, and perform special projects related to analytical and instrument problem-solving.

Requirements

Bachelor's or Master's Degree in Chemistry, Biology, Biochemistry, or related field
Generally requires minimal to no prior relevant work experience

Nice To Haves

Experience in a regulated industry (pharmaceutical, biotech, or medical devices).
Familiarity with GMP, GLP, and ISO standards.
Knowledge of analytical techniques such as spectroscopy, ELISA, IHC and microbiological testing.

Responsibilities

Conduct routine and non-routine analysis of raw materials, in-process items, and finished formulations.
Perform biochemical and/or chemical analyses to ensure stability and compliance with established procedures.
Compile data for documentation of test procedures, including assays and stability testing.
Calibrate and maintain laboratory equipment.
Participate in investigations and prepare summaries and reports.
Develop and validate testing methods as needed.
Review data for compliance with specifications and report abnormalities.
Revise and update standard operating procedures.
Perform special projects on analytical and instrument problem-solving.