Senior Manager or Associate Director, Supply Chain

<h3>Who we are:</h3> 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 <a href="https://www.kymeratx.com" target="_blank">www.kymeratx.com</a> or follow us on <a href="https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor" target="_blank">X (formerly Twitter)</a> or <a href="http://www.linkedin.com/company/kymeratherapeutics" target="_blank">LinkedIn</a>.    <h3>How we work:</h3> <ul> <li>PIONEER: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.</li> <li>COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.</li> <li>BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.</li> </ul>   <h3>How you’ll make an impact:</h3> We are seeking a Senior Manager/Associate Director of Supply Chain who will be responsible for managing and ensuring timely supply of materials for nonclinical and clinical studies at all stages of development. This role will be responsible for supply planning and execution for assigned projects, including demand forecasting, management of supply chain vendors, inventory management at depots and sites, packaging and labeling, import and export of drug substance and drug product, returns and destruction. The successful candidate can execute independently to ensure reliable supply for Kymera’s portfolio while also bringing the experience and judgment to help shape strategy, identify risks, and improve systems/processes as we scale.   This position reports to the Director, Supply Chain.   <ul> <li>Lead packaging, labeling, and distribution of clinical supplies from study initiation through closeout</li> <li>Develop and maintain clinical supply plans (forecast, timelines, and supply scenarios) in coordination with CMC and Clinical functions</li> <li>Coordinate and manage distribution of clinical trial material to depots and sites for clinical studies; monitor supply status and proactively mitigate risk.</li> <li>Manage clinical packaging/distribution vendors, including day-to-day oversight, issue resolution, review of batch documentation, and performance management (as applicable: support vendor selection and contract negotiations).</li> <li>Participate in the setup, testing and operation of interactive supply tracking systems (IRT) and other clinical supply tracking tools; ensure data accuracy and operational readiness.</li> <li>Represent the Supply Chain function on CMC and Clinical Study Teams and serve as the interface between the CMC and clinical teams to ensure smooth conduct of clinical studies.</li> <li>Coordinate import and export of materials to support clinical and non-clinical studies</li> <li>Materials management for GLP toxicology and clinical materials, including maintenance of inventory database and GxP documentation related to material receipt, storage and distribution</li> <li>Ensure compliance with industry standards, GMP, GDP, and applicable state and federal regulatory requirements; support audits/inspections as needed.</li> <li>Drive continuous improvement by standardizing processes, templates and metrics to improve visibility, cycle time, and reliability.</li> </ul>   <h3>Skills and experience you’ll bring:</h3> <ul> <li>BA/BS in Supply Chain/Operations or life sciences/health-related field.</li> <li>8+ years of experience in clinical supply chain management in the pharmaceutical industry, including global clinical trial supply operations</li> <li>Experience managing contract organizations for clinical labeling, packaging and distribution; ability to drive accountability through clear scope, timelines, and KPI’s</li> <li>Experience with clinical blinding practices and implementation/operation of IRT systems</li> <li>Knowledge of global and regional regulations pertaining to labeling and packaging, cGMP requirements and good distribution practices</li> <li>Working knowledge of import and export requirements, including proficiency in document preparation and international shipping logistics</li> <li>Ability to support, as needed, the investigation and resolution of complaints, product rejections, non-conformances, recalls, deviations, and trends from process performance</li> <li>Strong communication and stakeholder management skills; ability to work in a fast-paced environment while handling multiple priorities</li> </ul>                                                                                                                                                                                    <div>Equal Employment Opportunity</div> 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 <ul> <li>Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.</li> <li>The anticipated base salary range for this role is $145,000 – $240,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.</li> <li>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.</li> </ul>

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