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

We 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.

Responsibilities

• Execute 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 studies
• Implement process development (e.g. mixing optimization, TFF process optimization, buffer optimizations) in preparation for scaled-up production
• Perform 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 forward
• Maintain rigorous electronic laboratory records (ELN) and contribute to technical reports, patent applications, and future regulatory filings

Qualifications

• Research 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 experience
• Proven 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 preferred
• Hands-on experience in nanoparticle characterization tools and techniques related to nucleic acid quantification
• A rigorous approach to experimental planning and data analysis; attention to experimental details and ability to identify subtle deviations and troubleshoot formulation inconsistencies effectively
• Functional 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 stakeholders

Preferences 

• Familiarity 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 optimization
• Experience 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 environment

What We Offer 

• High-growth opportunity with meaningful impact on the future of protein design
• Competitive compensation package with equity participation
• 401(k) with a strong employer match
• Comprehensive benefits including health/dental/vision insurance
• Generous PTO policy and commitment to work-life balance
• Professional development opportunities in a cutting-edge field at the intersection of AI and biology

Profluent 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 Requirement

Applicants 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 Verification

Legal 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.