Scientist II, LNP, Process Development & Manufacturing

<div class="content-intro"><p>ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.</p></div><p> </p> <p><strong>The Role:</strong></p> <p>We are seeking a highly skilled LNP Scientist to join our process development team at ElevateBio. The ideal candidate will have hands-on experience in LNP formulation, targeted LNP (tLNP) engineering through bioconjugation, and a complete understanding of LNP-based processes. As an LNP Scientist, you will be responsible for designing and executing LNP formulation studies while also working closely with cross-functional teams and external clients for the manufacturing of LNP-based therapeutics. Your work will be critical in advancing the translation of LNP therapeutics from development through large-scale manufacturing at ElevateBio.</p> <p> </p> <p><strong>Here’s What You’ll Do:</strong></p> <ul> <li>Execute LNP production to support process characterization, technology transfer, and manufacturing readiness for LNP-based drug products.</li> </ul> <ul> <li>Work closely with cross-functional teams, including MSAT, AD, Quality, Manufacturing, and external clients, to support process development, scale-up and technology transfers.</li> <li>Characterize LNP and tLNP formulations using analytical techniques to evaluate size, PDI, encapsulation efficiency, lipid quantification, ligand density, conjugation efficiency, and formulation stability.</li> <li>Analyze and interpret experimental data, identify process improvement opportunities, and communicate technical findings, project updates, and recommendations to internal stakeholders and external clients.</li> </ul> <p> </p> <p> </p> <p><strong>Requirements: </strong></p> <p><strong>Education Requirements</strong></p> <ul> <li>Ph.D. in Pharmaceutical Sciences, Bioengineering, Biochemistry, Chemical Engineering, Biotechnology, Biomedical Engineering or a related discipline with 3+ years of industry experience in lipid nanoparticle (LNP) development or drug delivery, or M.S degree in a related field with 10+ years of relevant industry experience<strong>. Minimum of 3 years working with LNP-based products in a process development or manufacturing setting. </strong></li> </ul> <p><strong>Experience Requirements</strong></p> <ul> <li>Familiarity with GMP regulations, regulatory expectations, and preparation of technical documentation supporting CMC activities, technology transfer, and regulatory filings for LNP-based formulated products.</li> <li>Proven record of manufacturing LNP-based products through either process development work or tech transfer activities. </li> <li>Strong understanding and practical experience with LNP formulation, process development, including scale-up into GMP manufacturing with demonstrated expertise in LNP formulation development & optimization, tLNP development, and LNP purification.</li> <li>Ability to analyze and interpret data linking receptor engagement, ligand density, nanoparticle properties, cellular uptake, and delivery performance to guide tLNP optimization.</li> <li>Experience with LNP analytical and biophysical characterization techniques such as dynamic light scattering (DLS), zeta potential, encapsulation efficiency assays (e.g., RiboGreen), lipid quantification, and stability assessments.</li> <li>Experience operating automated LNP manufacturing and process development systems (e.g., PNI/Cytiva, Knauer) and filtration systems, including tangential flow filtration (TFF) platforms (e.g., Repligen).</li> <li>Ability to analyze complex experimental data, troubleshoot process challenges, and collaborate cross-functionally with MSAT, analytical development, manufacturing, and external partners.</li> </ul> <p> </p> <p><strong> </strong></p> <p><strong>Preferred Qualifications</strong></p> <ul> <li>Experience with targeted LNP development, including ligand conjugation strategies, functionalization approaches, and characterization of targeted delivery systems.</li> <li>Experience developing analytical methods for LNP characterization and release testing, including UPLC/HPLC-CAD for lipid analysis, payload quantification, and related analytical techniques.</li> <li>Working knowledge of mRNA process development unit operations including in-vitro transcription (IVT), chromatography (Affinity, RP, IEX), and integration with LNP formulation processes.</li> <li>Proficiency with statistical analysis software (e.g., JMP) and experience applying Design of Experiments (DoE) approaches and data-driven approaches to LNP formulation and process development.</li> </ul> <p> </p> <p><span data-teams="true"><em>The budgeted range for this position is $125,000 - $165,000. This range is a good faith estimate of the expected salary range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law. </em></span></p><div class="content-conclusion"><p><em>ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified