Quality Control Analyst - Second Shift

Agilent Technologies•Boulder, CO

About The Position

The Quality Control Analyst conducts routine and non-routine analyses and reviews analytical data for raw materials, in-process samples, finished products, microbiology and cleaning validation programs, and other requested testing. Work is performed according to standard operating procedures and analytical methods, current Good Manufacturing Practices (CGMP), and applicable regulatory requirements. The analyst completes projects and testing with supervision, applies knowledge of Good Laboratory Practices (GLP) and Good Documentation Practices (GDP), supports continuous improvement, and uses judgment to escalate issues to QC management and Quality Assurance. The role provides direct testing and reporting support to manufacturing, including meeting stringent schedules and deadlines. It performs analyses on clinical and commercial products, including biochemical and/or chemical analyses of raw materials, in-process materials, active pharmaceutical ingredients, and final products. The analyst reviews results against specifications, communicates with manufacturing, project managers, and QC management, supports laboratory investigations, and participates in routine laboratory and equipment maintenance. The role may also involve analytical and instrument troubleshooting, special projects, and mentoring or training others. This is a full-time second-shift position with a Monday–Friday schedule from 2:30 p.m. to 11:00 p.m. Travel is not required. The stated full-time equivalent pay range is $34.00–$53.13 per hour, with eligibility for bonus, stock, and benefits. Applications are accepted until at least October 30, 2026, or until the job is no longer posted.

Requirements

Bachelor of Science degree in Chemistry, Biology, or a related stated field.
At least 1–2+ years of relevant experience in analytical chemistry or a related life sciences industry field, or an equivalent combination of education, training, and experience.
Knowledge of analytical equipment and instrumentation, including UV-Vis, Karl Fischer, HPLC/HPLC-MS, and pH.
Ability to efficiently, accurately, and independently execute day-to-day tasks with minimal supervision.
Knowledge of computer software and hardware applications, including Microsoft Word and Excel.

Nice To Haves

Experience in CGMP, CDMO, and/or pharmaceutical settings.
Familiarity with Agilent instrumentation and software.
Knowledge of FDA and international regulations and guidelines, including USP, JP, EP, and ICH.

Responsibilities

Test and report data for in-process samples to support manufacturing while meeting schedules and deadlines.
Perform analyses of clinical and commercial products under CGMP regulations and applicable FDA and international guidance.
Conduct biochemical and/or chemical analyses of raw materials, in-process materials, active pharmaceutical ingredients, final products, and other requested samples according to established procedures.
Collaborate and communicate with manufacturing, project managers, and QC management.
Review data for compliance with specifications and report or escalate abnormalities as necessary.
Follow good documentation practices.
Work cross-functionally to complete projects and testing.
Support laboratory investigations and reports.
Participate in routine laboratory and equipment maintenance.
Perform special projects involving analytical and instrument problem-solving and troubleshooting, as needed.
Assist with mentoring or training others, as appropriate.