Agilent Technologies

ResearchAssociate,AnalyticalChemistry

$69–108k Frederick, Colorado, United States FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Research Associate, Analytical Chemistry at Agilent Technologies. Skills: Analytical Chemistry, Method Validation, API Manufacturing. Execute analytical techniques. Author method validation protocols”

Industry & Context.

Problems you'll solve

Troubleshoot instrumentation; Troubleshoot method issues

Eligibility Requirements

Occasional travel, Day shift

What They're Looking For.

Must Have

Bachelor's in chemistry, 1 year relevant experience, Experience in following SOPs, Experience with HPLC/UPLC, Experience with HPLC-MS

Nice to Have

Experience in cGMP regulated environment, Experience with method validation, Ability to work with interdisciplinary project teams, Understand project requirements, Follow project timelines

What You'll Do.

Execute analytical techniques

Author method validation protocols

Author method validation reports

Conduct laboratory scale experiments

Record and summarize experiments

Construct research summaries

Maintain process compliance integrity

Operate laboratory equipment

Troubleshoot instrumentation

Troubleshoot method issues

Perform preventative maintenance

How You'll Work.

Team & Collaboration

Present to internal teams; Work with interdisciplinary teams

Communication Scope

Present research summaries

Full Job Description

## **Job Description** Agilent Technologies Nucleic Acids Solutions Division is looking to add a Research Associate to their Analytical Services team in the Development department at their contract Active Pharmaceutical Ingredient (API) manufacturing facility, located in Boulder, Colorado, that specializes in oligonucleotide chemistries. As a Research Associate in the Analytical Services team the candidate will be responsible for executing analytical techniques in support of method validation used in supporting Active Pharmaceutical Ingredient (API) manufacturing. Responsibilities: * Design and conduct laboratory scale experiments using analytical instrument platforms such as HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, Karl Fischer * Author method validation protocols and reports with adherence to ICH guidelines and internal Agilent standard operating procedures (SOPs) * Design and safely conduct laboratory scale experiments using current best practices for API testing * Properly record and summarize experiments in notebooks and reports and construct research summaries to present to internal teams * Maintain process compliance integrity by adhering to SOPs and current good manufacturing practices (cGMP) as appropriate. * Operate laboratory equipment by following operating instructions, troubleshooting instrumentation and method issues, and performing routine preventative maintenance ## ## **Qualifications** **Required:** * Bachelor's (B.S.) or equivalent in chemistry * 1 year relevant experience and/or training * Experience in following SOP’s for analytical method execution such as HPLC/UPLC, HPLC-MS **Desired:** * Experience in cGMP regulated environment * Knowledge of ICP-MS, IC, GC, GC-MS, UV, Karl Fischer is desired * Knowledge of analytical test methods used in the testing of oligonucleotide API or related molecules is highly desired * Experience with method validation * Ability to work with interdisciplinary project teams, understand project requirements, a

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