Scientist IAt Avidity Biosciences, we are passionate about the impact of every employee in realizing our vision of improving people's lives by delivering a new class of RNA therapeutics. Avidity is revolutionizing the field of RNA with its proprietary AOCs, which are designed to combine the specificity of monoclonal antibodies with the precision of oligonucleotide therapies to address targets and diseases previously unreachable with existing RNA therapies. If you are a committed, solution-oriented thinker, join us in making a difference and become part of our growing culture that is integrated, collaborative, agile and focused on the needs of patients.We are seeking a highly motivated individual eager to work in a fast-paced and collaborative environment as a Scientist I within the Analytical and Formulation group of Avidity's Technical Development and Operations (TD&O) department. This position will focus primarily on the clinical and commercial formulation development of AOC drug product and drug substance. Additional responsibilities may include but are not limited to supporting the developability assessments of early-stage mAb and AOC assets and performing in-use compatibility studies for intravenous and subcutaneous routes of administration. The successful candidate will have a strong scientific background and demonstrated experience in analytical and biophysical characterization.
Experience in formulation development and stability testing of protein biologics, particularly for mAbs and antibody-drug conjugates (ADCs), is highly desirable. Strong interpersonal, organizational, and communication skills are essential as this position will require close collaboration with cross-functional team members as well as periodic communication with external research organizations and vendors. This position will report to the Principal Scientist within the Analytics and Formulation group, which is laboratory-based at the Avidity site in San Diego, CA. Non-laboratory functions such as data processing and documentation, however, may be completed remotely.What You Will ContributeDesign and work with TD&O team members to set up and conduct formulation stability studies of mAb and AOC liquid and lyophilized dosage formsConduct in-use compatibility studies of AOC drug products intended for intravenous and subcutaneous routes of administrationPerform developability assessments of numerous early-stage protein biologics using a variety of predictive analytical and biophysical methodsCarry out routine lab tasks including preparing buffers, managing the inventory of laboratory consumables and supplies when neededWork with vendors for maintenance and troubleshooting of analytical instrumentsSupport mAb and AOC drug substance/product process development activities when neededBe a hands-on presence in the laboratory and support biology and chemistry departments with analytical and biophysical characterization as neededTrain lab personnel on the use of select instrumentation and methodsSpecify, purchase, and manage the installation of formulation-related instrumentation and equipmentMaintain good documentation in an electronic notebook and write technical reports as requiredPresent data at regular team and cross functional team meetingsContributes to the company's core values (agile, visionary, integrated and diverse)What We SeekA PhD in chemistry, biology, pharmaceutical sciences, or a related field (master's or bachelor's degree with 5 and 10 years industry experience, respectively, will be considered).An in-depth understanding of protein physicochemical stability, particularly how solvent conditions and cosolutes impact protein colloidal, conformational and chemical stabilities.Hands-on experience with a variety of analytical methods including SEC, IEX, RP-HPLC, CE-SDS, cIEF and subvisible particle analysisExperience using a variety of biophysical methods for characterizing and measuring conformational and colloidal stability of protein biologics including differential scanning calorimetry, dynamic and static light scattering techniquesAbility to design, implement and analyze formulation studies using a one-factor at a time and design of experiment (DOE) approaches using JMP statistical software or similarAbility to multi-task and work in a fast-paced cross-functional matrix environmentDemonstrated excellent communication (oral and written), teamwork, organizational, interpersonal, and problem-solving skillsDirect experience in any of the areas listed below would be viewed favorably but are not a requirement for the position:Familiarity with mass spectrometry (MS) methods used for assessing mAb chemical stability and assessing ADC drug to antibody ratios including intact, reduced, and peptide mapping LC/MSPrior experience in lyophilization formulation, cycle development, and analytical testingExperience in oligonucleotide chemistry and characterization methodsExperience working with external CMOs and CROsPrevious experience managing direct reportsWhat We Will Provide To You:The base salary range for this role is $127,300-$140,700. The final compensation will be commensurate with such factors as relevant experience, skillset, internal equity and market factors.Avidity offers competitive compensation and benefits, which includes the opportunity for annual bonus as well as a 401(k) with an employer match. In addition, the comprehensive wellness program includes coverage for medical, dental, vision, and LTD, and four weeks of time off.A commitment to learning and development which includes a variety of programming internally developed by and for Avidity employees, opportunities for job-specific training offered by industry, and an education reimbursement program.Location: Hybrid - San Diego, CA and RemotePosition Type: Full Time / ExemptDepartment: Analytical Development & Formulation