Specialist or Manager, Quality Systems

Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit or follow us on X (formerly Twitter) or LinkedIn. How we work: PIONEER : We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines. COLLABORATE : We value trust transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine. BELONG : We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard. How you’ll make an impact: The Quality Systems role is responsible for managing the operational infrastructure of Kymera’s Quality Management System, with primary ownership of document control, training program management, and quality systems compliance monitoring. This role ensures that GxP-controlled documents, SOPs, and personnel training records are accurately maintained and compliant with applicable regulatory requirements. The individual will play a key role in sustaining day-to-day QMS operations, managing the controlled document lifecycle including biennial review programs, driving training compliance across the organization, and supporting quality systems performance monitoring as Kymera advances late-stage development and commercialization. Administer and maintain Kymera’s Document Control and Training electronic Quality Management System (Veeva Vault) Manage document lifecycle, review/approval workflows, archiving, retrieval and biennial review across all GxP functions Develop and maintain role-based GxP training curricula, assign training tasks upon document approval, and monitor compliance across the organization to meet defined quality objectives Track and report QMS metrics to support Quality Management Review and executive reporting Maintain inspection-ready training records, document retrieval indexes, and controlled document inventories Contribute to the development, revision, and lifecycle management of Quality System SOPs and policies in alignment with Kymera’s QMS Maintain vendor qualification records and Approved Supplier List Support quality systems compliance monitoring activities and contribute to continuous improvement of QMS infrastructure as Kymera scales towards late stage and commercialization Skills and experience you’ll bring: Bachelor’s degree in Life Sciences, or related field required 5 years of experience in Quality Systems, Document Control, or GxP Quality in a sponsor organization Hands-on experience administering an electronic document management or eQMS platform Experience managing GxP training programs including curriculum maintenance, training matrix administration, and compliance tracking in a regulated environment Working knowledge of 21 CFR Part 11, ICH E6(R3), and GxP document control and training Familiarity with quality systems elements including CAPA, deviations, audits, and vendor qualification Experience supporting regulatory inspection readiness activities is a plus Strong organizational skills with ability to manage multiple concurrent document workflows and priorities in a fast-paced environment High attention to detail, clear written and verbal communication skills with ability to engage cross-functional stakeholders at all levels Self-directed with ability to prioritize workload and elevate appropriately Proficient in Veeva Vault, Microsoft Office suite including Word, Excel, and PowerPoint Equal Employment Opportunity Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class. Compensation Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay. The anticipated base salary range for this role is $85,000 - $200,000, with eligibility for annual bonus, equity participation, and comprehensive benefits. Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position. #J-18808-Ljbffr Kymera Therapeutics