Research Associate/Sr. Research Associate - Process Development/Manufacturing

Research Associate/Sr. Research Associate – Process Development/ManufacturingCellics Therapeutics is a rapidly growing biotech company developing novel therapeutics for inflammatory and infectious diseases based on the award-winning Cellular Nanoparticle technology. Cellics offers a highly motivational and rewarding work environment with attractive salary and benefits.Base pay range$70,000.00/yr - $90,000.00/yrAnnual Bonus and Stock optionsAbout the RoleWe are seeking a Research Associate/ Senior Research Associate of Downstream process development/manufacturing to join the CMC team. The candidate will contribute to the design and development of the manufacturing process and the manufacturing of DS/DP to support the pre-clinical and clinical trial studies.ResponsibilitiesDesign and develop scale-up Downstream process for manufacturing nanoparticle-based drug substance and drug product.Perform analysis of experimental data and interpret immediate experimental outcomes and/or conclusions within established protocols.Act as the lead in daily operations ensuring all components are in place and all documentation is complete prior to finishing a campaign.Act as SME (subject matter expert) for a specific piece of equipment.Schedule and execute manufacturing tasks under cGMP guidelines.Troubleshoot manufacturing processes under cGMP guidelines and under the supervision of manufacturing supervisor.Assist in the research and implementation of new methods and technologies to enhance operations.Prepare components, buffers, and other solutions as needed.Accurately document data and write/review batch records under cGMP guidelines.Reliably execute and write well defined SOPs and manufacturing batch records.Initiate and write revisions to current GMP/SOP guidelines.Responsible for routine maintenance of production equipment and production suites.RequirementsBachelor's or Master's degree in Chemistry, Chemical Engineering, Biology, or related field.1+ years of experience (for RA), or 2+ years experience (for Senior RA) working in a cGMP or process development environment strongly preferred.Experience in Tangential Flow Filtration, Depth Filtration, and Microfluidization.Strong critical thinking and problem-solving skills.Energetic, positive, self-motivated, and hands-on professional with strong work ethics, able to work both independently and with a team in an intense, data-driven, and interrogative environment.Strong written and verbal communication skills.May be required to lift up to 25 pounds.BenefitsMedical insuranceVision insurance401(k)J-18808-Ljbffr