Research Associate II - Senior Research Associate II, LNP Formulation & Drug Delivery

Company OverviewProfluent is an AI-first protein design company. Founded in 2022, we develop deep generative models to design and validate novel, functional proteins to revolutionize biomedicine. Based in Emeryville, CA, we are backed by leading investors including Altimeter Capital, Bezos Expeditions, Spark Capital, Insight Partners, Air Street Capital, AIX Ventures, and Convergent Ventures, and have raised over $150M to date.The RoleWe are seeking a highly motivated and innovative researcher to join our LNP Formulation team. This role is central to our mission of advancing next-generation gene editing therapies. You will play a pivotal role in the formulation, characterization, and optimization of Lipid Nanoparticle (LNP) delivery systems, transitioning breakthrough AI-designed gene editors from the bench to in vivo applications. The ideal candidate will have extensive hands-on experience with LNP formulation, process development and LNP characterization. This is an excellent opportunity to work cross-functionally with a diverse team of experts across AI and machine learning, protein design, cell biology, and gene editing.ResponsibilitiesExecute the formulation of LNPs encapsulating diverse gene editing payloads (mRNA, sgRNA) for in vitro validation and in vivo preclinical studies. Optimize LNP potency by conducting Design of Experiments (DOE) type of studiesImplement process development (e.g. mixing optimization, TFF process optimization, buffer optimizations) in preparation for scaled-up productionPerform routine and advanced LNP analytics, including particle size/polydispersity (e.g., dynamic light scattering), zeta potential, pKa determination, and encapsulation efficiency (e.g., RiboGreen assays)Collaborate closely with internal therapeutics translation teams and external CROs to advance multiple programs forwardMaintain rigorous electronic laboratory records (ELN) and contribute to technical reports, patent applications, and future regulatory filingsQualificationsResearch Associate II: BS with 2+ years of relevant industry experience. Senior Research Associate: MS with 2-4 years; OR BS with 4-6 years of relevant industry experienceProven hands-on experience with LNP production (e.g., microfluidic mixing, T-junction) and purification techniques (TFF, dialysis)Must have at least 2 years of experience working in an industry lab; 4+ years preferredHands-on experience in nanoparticle characterization tools and techniques related to nucleic acid quantificationA rigorous approach to experimental planning and data analysis; attention to experimental details and ability to identify subtle deviations and troubleshoot formulation inconsistencies effectivelyFunctional proficiency in GraphPad Prism for data analysis, including generating scientific graphs and performing routine statistical tests (e.g., t-tests and ANOVA)Excellent verbal and written skills with a demonstrated ability to summarize complex datasets for diverse stakeholdersPreferencesFamiliarity with automation or robotic platforms for rapid formulation library generation.Practical knowledge of DOE (Design of Experiments) software such as JMP or Design-Expert for systematic formulation screening and optimizationExperience with LC-based analysis tools for lipids and RNA (e.g., HPLC/UPLC, UPLC-CAD)An agile, "growth-oriented" approach with the ability to pivot and adapt to the evolving needs of an early-stage research environmentWhat We OfferHigh-growth opportunity with meaningful impact on the future of protein designCompetitive compensation package with equity participation401(k) with a strong employer matchComprehensive benefits including health/dental/vision insuranceGenerous PTO policy and commitment to work-life balanceProfessional development opportunities in a cutting-edge field at the intersection of AI and biologyProfluent Bio, Inc is an equal opportunity employer promoting diversity and inclusion in the workspace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical conditions, veteran status, sexual orientation, gender (including gender identity and gender expression), sex (which includes pregnancy, childbirth, and breastfeeding), genetic information, taking or requesting statutorily protected leave, or any other basis protected by law.Work Authorization RequirementApplicants must have ongoing work authorization in the United States that does not require employer sponsorship. Sponsorship will not be provided now or at any time in the future for this position.Employment Eligibility VerificationLegal authorization to work in the United States is required. In compliance with federal law, all persons hired must verify their identity and work eligibility and complete the required employment verification form upon hire.