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 include designing and conducting laboratory scale experiments using analytical instrument platforms such as HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, Karl Fischer; authoring method validation protocols and reports with adherence to ICH guidelines and internal Agilent standard operating procedures (SOPs); designing and safely conducting laboratory scale experiments using current best practices for API testing; properly recording and summarizing experiments in notebooks and reports and constructing research summaries to present to internal teams; maintaining process compliance integrity by adhering to SOPs and current good manufacturing practices (cGMP) as appropriate; operating laboratory equipment by following operating instructions, troubleshooting instrumentation and method issues, and performing routine preventative maintenance. Qualifications include a Bachelor's (B.S.) or Master's Degree or equivalent in chemistry or related applied sciences field, 8+ years relevant experience and/or training or equivalent combination of education and experience, experience in following SOP’s for analytical method execution such as HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, Karl Fischer is highly desired, knowledge of analytical test methods used in the testing of oligonucleotide API or related molecules is highly desired, and ability to work with interdisciplinary project teams, understand project requirements, and follow project timelines.
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