Agilent Technologies
ResearchAssociate,AnalyticalChemistry
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Research Associate, Analytical Chemistry at Agilent Technologies. Skills: Analytical Chemistry, Method Validation, API Manufacturing. Execute analytical techniques. Author method validation protocols”
Industry & Context.
Troubleshoot instrumentation; Troubleshoot method issues
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
Applying for this Research Associate, Analytical Chemistry role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Agilent Technologies?
Real rants from real employees. Read before you apply.