Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Обязанности описаны чётко, а работа даёт практический опыт с аналитикой РНК и LNP; при этом стоит учесть работу на месте и широкий набор лабораторных методов.
?Широкий набор методов
Перспективная специализация
Понятные обязанности
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Research Associate, Analytical Development (RNA/LNP) (HPLC/UHPLC, LC-MS, Flow Cytometry): Developing and executing analytical methods for RNA, lipids, lipid nanoparticles, and related bioconjugates with an accent on chromatography, mass spectrometry, nano flow cytometry, and wet-lab sample preparation. Focus on characterizing RNA and LNP quality attributes, troubleshooting analytical workflows, reviewing data, and supporting method optimization and transfer.
Location: Onsite in Seattle, Washington, United States
Salary range: $65,000–$80,000 annual total compensation, including bonus, depending on experience and qualifications.
Company
hirify.global is a biotechnology company providing research and development services and biological building blocks for healthcare and life-science applications.
What you will do
Prepare RNA, oligonucleotide, lipid, LNP, antibody, and bioconjugate samples for analytical testing.
Perform HPLC/UHPLC analyses, including sample and standard preparation, sequence setup, chromatogram review, peak integration, and initial data assessment.
Support LC-MS characterization of RNA, oligonucleotides, synthetic cap analogs, lipids, and related materials, including sample preparation, spectral review, and data processing.
Perform RNA and LNP analytical testing for concentration, purity, integrity, aggregation, lipid composition, and residual components.
Execute nano flow-cytometry workflows, including fluorescent sample preparation, instrument QC, acquisition, gating, and targeted LNP characterization.
Maintain laboratory records, process data, support SOPs and method transfer, troubleshoot instruments and workflows, and collaborate with R&D, QC, and Production.
Requirements
Bachelor’s degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, Biotechnology, Pharmaceutical Sciences, or a related scientific discipline.
0–5 years of relevant academic or industry laboratory experience, preferably in analytical chemistry, biopharmaceutical characterization, nucleic acid analysis, or a related field.
Hands-on experience with HPLC/UHPLC and/or LC-MS, including sample preparation, established method execution, and basic chromatographic or analytical data review.
Practical flow-cytometry experience, including fluorescent sample preparation, controls, data acquisition, and basic gating or data interpretation.
Strong wet-lab skills in accurate pipetting, solution and buffer preparation, dilution calculations, sample handling, and contamination control.
Ability to follow written procedures accurately and maintain clear, complete, and traceable laboratory records.
Ability to use Microsoft Excel or similar tools to organize, analyze, and summarize experimental data.
Strong attention to detail, organization, problem-solving ability, willingness to learn, and ability to manage multiple sample batches and priorities.
Ability to communicate progress, results, and technical issues clearly and collaborate in a multidisciplinary R&D environment.
Nice to have
Master’s degree in Analytical Chemistry, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline.
Experience with mRNA, circRNA, oligonucleotides, lipids, LNPs, antibodies, or bioconjugates.
Experience with HPLC-CAD, SEC, ion-pair reversed-phase or ion-exchange chromatography, preparative HPLC, or RNA gel/capillary electrophoresis.
Experience with LC-MS characterization of nucleic acids, oligonucleotides, cap structures, lipids, or related biomolecules.
Experience with small-particle or nanoparticle flow cytometry, including platforms such as Beckman Coulter CytoFLEX nano.
Familiarity with Agilent, Waters, or Thermo Scientific analytical instrumentation and software such as Empower, Xcalibur, BioPharma Finder, or CytExpert.
Understanding of analytical method development, qualification, transfer, or troubleshooting in an R&D, biotechnology, pharmaceutical, CRO, or CDMO environment.
Culture & Benefits
Onsite role at the Seattle site with cross-functional collaboration across R&D, QC, Production, and related teams.
Medical, dental, and vision insurance, plus a 401(k) plan with company match fully vested on day one.
Paid parental leave after three months and paid vacation, personal, sick, floating-holiday, and company-holiday time.
Flexible spending and health savings accounts, disability and life insurance, legal assistance, supplemental insurance, commuter benefits, and well-being initiatives.
Free colleague meals during shifts and onsite gyms.
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