Research Associate, Analytical Development
BioSpace
Posted 14 Nov 2026, 00:46 ET
This job at a glance
- Who can apply
- New grads and up to 5 years · Bachelor's degree or Master's degree
- Must know
- Data analysisExcelOperations
- Nice to have
- CADTroubleshooting
- Work
- On-site in Seattle
- Pay
- $65K–$80K a year
- Skill demand
- Operations31%Data analysis26%Excel17%of 99 similar entry-level jobs posted in the US this week
- Listed
- Nov 14, 2026 · still open
Sign in free to see which of these skills your resume already shows.
About the Role
BioSpace is seeking a motivated and detail-oriented Research Associate, Analytical Development to support the development, qualification, and routine execution of analytical methods for RNA, lipids, lipid nanoparticles (LNPs), and related bioconjugates.
Key Responsibilities
-
Chromatography and Analytical Testing
-
Prepare RNA, oligonucleotide, lipid, LNP, antibody, and bioconjugate samples for analytical testing.
-
Perform HPLC/UHPLC analyses using UV and/or charged aerosol detection (CAD).
-
Support chromatographic methods for evaluating RNA purity, lipid identity and purity, lipid composition, residual components, and related product-quality attributes.
-
Assist with preparative chromatography, fraction collection, sample tracking, and evaluation of purification fractions for RNA and related development projects.
-
Support analytical method development, optimization, troubleshooting, and transfer.
-
LC-MS Characterization
-
Support LC-MS characterization of RNA, oligonucleotides, synthetic cap analogs, and related materials.
-
Assist with characterization of attributes such as molecular identity, capping efficiency, and poly(A) characteristics.
-
Perform sample preparation and assist with spectral review, data processing, and interpretation.
-
Support troubleshooting of sample-preparation, chromatographic, mass-spectrometric, and data-processing issues.
-
RNA and LNP Analytical Development
-
Perform analytical testing to support characterization of mRNA, circRNA, oligonucleotides, lipids, LNPs, antibodies, and related bioconjugates.
-
Support assays evaluating RNA attributes such as concentration, purity, integrity/fragmentation, aggregation, and residual process-related components.
-
Support characterization of LNP-related attributes, including lipid composition and purity and residual/free components associated with LNP conjugation or formulation processes.
-
Perform routine sample cleanup, dilution, buffer preparation, and analytical sample processing using appropriate RNase-free techniques.
-
Nano Flow Cytometry and Targeted LNP Characterization
-
Prepare fluorescently labeled samples, standards, and appropriate experimental controls for flow-cytometry analysis.
-
Perform routine flow cytometer setup, instrument QC, sample acquisition, and application of established analysis and gating strategies.
-
Support characterization of antibody-decorated or targeted LNPs, including evaluation of labeling and conjugation-related attributes.
-
Assist with optimization and troubleshooting of flow-cytometry-based analytical workflows.
-
Laboratory Execution and Data Analysis
-
Perform routine wet-lab activities requiring accurate pipetting, serial dilution, buffer and reagent preparation, concentration measurements, and sample cleanup.
-
Process analytical results using relevant instrument software and Microsoft Excel or equivalent data-analysis tools.
-
Review results for consistency and data quality, prepare clear data summaries, and promptly communicate unexpected findings, deviations, or instrument issues.
-
Maintain accurate, complete, and traceable experimental documentation, sample records, reagent inventories, and laboratory records.
-
Laboratory Operations and Cross-Functional Support
-
Support preparation and revision of SOPs, test methods, work instructions, and analytical documentation.
-
Assist with routine instrument maintenance, laboratory organization, and method-transfer activities.
-
Collaborate effectively with scientists and colleagues across R&D, QC, Production, and related functional teams.
-
Follow applicable laboratory safety procedures, chemical-handling requirements, and site EHS policies.
-
Contribute to continuous improvement of analytical workflows, laboratory efficiency, data quality, and technical capabilities.
Requirements & Tech Stack
- Hands-on experience with HPLC/UHPLC and/or LC-MS, including sample preparation, execution of established analytical methods, and basic chromatographic or analytical data review.
- Practical experience with flow cytometry, including fluorescent sample preparation, use of appropriate controls, data acquisition, and basic gating or data interpretation.
- Strong fundamental wet-lab skills, including accurate pipetting, solution and buffer preparation, dilution calculations, sample handling, and contamination control.
- Ability to follow written procedures and experimental protocols accurately and maintain clear, complete, and traceable laboratory records.
- Ability to use Microsoft Excel or similar software to organize, analyze, and summarize experimental data.
- Strong attention to detail, organization, problem-solving ability, and willingness to learn new analytical technologies.
- Ability to manage multiple sample batches and experimental priorities while communicating progress, results, and technical issues clearly.
- Ability to work collaboratively in a multidisciplinary R&D environment.
Qualifications
- 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.
Preferred Qualifications
- Master's degree in Analytical Chemistry, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline.
- Previous experience working with mRNA, circRNA, oligonucleotides, lipids, LNPs, antibodies, or bioconjugates.
- Experience with analytical techniques such as HPLC-CAD, SEC, ion-pair reversed-phase chromatography, 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, particularly platforms such as the Beckman Coulter CytoFLEX nano.
- Familiarity with Agilent or Waters HPLC/UHPLC systems, Thermo Scientific LC-MS platforms, or related analytical instrumentation.
- Experience using analytical 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.
Compensation
Salary range: $65,000 – $80,000 total compensation, including bonus, depending on experience and qualifications.
Benefits
- Medical, dental, and vision insurance.
- 401(k) retirement plan with a company match that vests fully on day one.
- Paid parental leave after three (3) months of employment.
- Paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays.
- Flexible spending and health savings accounts.
- Life and AD&D insurance, short- and long-term disability coverage.
- Legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance.
- Commuter benefits, well-being initiatives, and peer-to-peer recognition programs.