Agilent Technologies is expanding its Colorado operations to support the development and commercialization of nucleic acid therapeutics. The Quality Control Analyst conducts routine and non-routine analysis and reviews to support in-process testing in accordance with Standard Operating Procedures (SOPs), analytical methods, current Good Manufacturing Practices (cGMPs), and regulatory requirements. The role requires understanding of Good Laboratory Practices (GLPs), cGMPs, and other applicable regulations, along with sound judgment and appropriate escalation of issues to QC management. The analyst contributes to continuous improvement and communicates effectively with management. The position follows a Monday-to-Friday second-shift schedule, with a choice of either 1:30 p.m. to 10:00 p.m. or 2:30 p.m. to 11:00 p.m. It is a full-time role. The listed full-time-equivalent pay range is $34.00–$53.13 per hour, with eligibility for bonus, stock, and benefits. Actual pay depends on work location and job-related factors such as skills, experience, and education or training.
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Job Type
Full-time
Career Level
Mid Level