Sr. Manager, QC LIMS Administrator

At Viridian, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets.Reporting to the Executive Director, Quality Control, the Sr. Manager, QC LIMS Administrator will serve as a key subject matter expert responsible for configuring, maintaining, and optimizing the LIMS platform to support Quality Control laboratory operations. This role will collaborate closely with stakeholders across IT, Analytical Development (AD), Quality Control (QC), Quality Assurance (QA), and Computer System Validation (CSV) to ensure compliant, efficient, and user-friendly system solutions. The LIMS Administrator will lead system configuration projects, support data integrity initiatives, manage routine updates, and provide user training to enable reliable and streamlined laboratory operation.Responsibilitieso):Lead the configuration, maintenance, and enhancement of QC workflows within the LIMS platformTranslate user and business requirements into effective, compliant system solutions and workflowsDevelop and execute projects and implement plans to ensure timely delivery of enhancementsOwn and manage change controls, deviations, and other quality records related to LIMSServe as QC lead for metadata management, reporting, and data structure updatesAuthor and deliver end-user procedures, training materials, and hands-on training sessionsSupport system upgrades, validation activities, and ensure ongoing system compliance with regulatory requirementsGenerate and manage LIMS data reporting and support data queries from business partnersPartner with IT and vendors to troubleshoot, escalate, resolve LIMS issuesSupport internal and external audits by ensuring data integrity and system compliance with applicable regulatiQualificationsns:Requires a Bachelor's degree in Life Sciences, Computer Science, Information Technology, or a related field with 8+ years of relevant experience in the life sciences, biotech, or pharmaceutical industryStrong understanding of QC laboratory workflows, analytical instrumentation, and data management principlesIn-depth knowledge of data integrity regulations and guidelines (21 CFR Part 11, Computer System Validation, ALCOA++)Proven hands-on experience in LIMS administration, configuration, implementation, and validationAbility to translate user requirements into efficient system workflows and develop creative solutions within platform constraintsExcellent communication skills with the ability to train and support staff across multiple levels and functionsDemonstrated project management experience and ability to work in a fast-paced, collaborative environmentComfortable in an adaptable small company environment with minimal direction and able to adjust workload based upon changing prioritiesStrong commitment to ethical standardsProficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)Ability to travel up to 5%The salary range for this position is commensurate with experienceViridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.Seniority levelMid-Senior levelEmployment typeFull-timeJob functionQuality AssuranceJ-18808-Ljbffr