Cabaletta Bio

Coordinate and monitor shipments of patient and manufacturing materials across the cell and gene therapy supply chain ensuring timely and compliant delivery. | Experience in logistics coordination, knowledge of chain of custody, temperature-controlled transportation, and ability to manage international shipments and stakeholder communication. | Philadelphia, PA (Remote) Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on developing and launching targeted, potentially curative, cellular therapies for patients with autoimmune diseases. The CABA™ platform includes two strategies to treat and potentially cure many of the most common and challenging autoimmune diseases. The CARTA strategy, or Chimeric Antigen Receptor T cells for Autoimmunity, is designed to potentially reset the immune system by causing transient B cell depletion with early academic clinical data suggesting the potential of this strategy to transform treatment in patients with SLE and the possibility of cures in rheumatoid arthritis, myositis, and systemic sclerosis, among others. Our lead product candidate using the CARTA strategy is CABA-201, 4-1BB-containing CD19-CAR T designed specifically to treat patients with autoimmune diseases and which uses a CD-19 binder that has an encouraging clinical tolerability profile. The second strategy is Cabaletta Bio’s proprietary CAART, or chimeric autoantibody receptor T cells, strategy, which is designed to cause antigen-specific B cell depletion of well-defined, disease-causing B cells. Our lead product candidate developed using the CAART strategy is being evaluated in a clinical trial for patients with mucosal pemphigus vulgaris (mPV) and our second product candidate is expected to initiate a clinical trial later this year in muscle-specific tyrosine kinase (MuSK) myasthenia gravis. Cabaletta Bio’s headquarters are located in Philadelphia, PA. For more information, visit www.cabalettabio.com and follow us on LinkedIn and Twitter. Uniquely Differentiated. Rapid. Elegant. At Cabaletta, we are driven by the shared mission of developing cures, where a patients’ own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew. We’re proud to be a Great Place to Work-Certified™ company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Work® About The Position The Logistics Coordinator is responsible for the coordination, booking, tracking, and communication of all patient material, manufacturing material, and finished product shipments across the cell and gene therapy supply chain. This role serves as a central point of contact between treatment centers, manufacturing sites, couriers, depots, and internal stakeholders to ensure timely and compliant movement of critical patient-specific materials. The Logistics Coordinator proactively monitors shipments, manages transportation milestones, communicates status updates, and escalates risks to support uninterrupted patient treatment schedules. Responsibilities Shipment Coordination & Booking • Coordinate domestic and international transportation bookings for patient leukapheresis collections, starting materials, intermediates, and finished drug products. • Schedule and confirm shipments with approved specialty logistics providers and courier partners. • Ensure transportation arrangements align with manufacturing schedules, patient treatment dates, and chain of identity/chain of custody requirements. • Prepare and review shipping documentation, customs paperwork, and transportation instructions as required. • Verify shipment readiness and ensure all required packaging, labeling, and documentation are available prior to dispatch. Shipment Tracking & Monitoring • Monitor shipments from pickup through final delivery using transportation management systems and courier tracking platforms. • Provide proactive oversight of critical patient shipments to ensure adherence to planned timelines and temperature requirements. • Investigate transportation delays, route deviations, temperature excursions, and delivery issues. • Coordinate corrective actions with logistics providers and internal stakeholders to minimize patient impact. • Maintain accurate shipment records and tracking information in designated systems. Communication & Stakeholder Management • Serve as the primary communication point for shipment status updates across internal and external stakeholders. • Provide timely updates regarding shipment milestones, exceptions, and potential risks. • Coordinate communication between treatment centers, manufacturing facilities, couriers, quality teams, scheduling teams, and patient operations groups. • Facilitate escalation management for critical transportation events and ensure rapid stakeholder notification. • Participate in daily operational meetings and provide shipment status reports. Operational Excellence & Compliance • Ensure all logistics activities comply with GDP, GMP, GxP, IATA, DOT, and applicable regulatory requirements. • Maintain chain of identity and chain of custody documentation throughout the transportation process. • Support deviation investigations and root cause analysis related to shipment exceptions. • Contribute to SOP development, process improvements, and continuous improvement initiatives. • Monitor logistics performance metrics and assist in developing corrective and preventive actions. Preferred Qualifications • Experience in cell and gene therapy, biopharmaceutical, clinical trial, or healthcare logistics. • Knowledge of chain of custody and chain of identity requirements. • Familiarity with cryogenic and temperature-controlled transportation. • Experience managing international shipments and customs documentation. • Experience with transportation management systems (TMS) or logistics control toweroperations. Key Competencies • Attention to detail • Customer and patient focus • Sense of urgency • Problem solving and critical thinking • Cross-functional collaboration • Risk identification and escalation management • Time management and prioritization • Adaptability in a fast-paced environment Our name – Cabaletta – is derived from the operatic term for the second part of an aria that is designed to highlight the technical expertise of the lead singer. While our company is not the first to develop chimeric T cells as therapies, we are the first to develop them in a way that leverages T cells to specifically eliminate only B cells that cause disease, while sparing healthy B cells. Utilizing the backbone of this core technology, we expect to advance our portfolio with a rapid and repetitive rhythm, similar to the rhythm that is typical of a cabaletta. For more information, please visit https://www.cabalettabio.com/ or email careers@cabalettabio.com directly to apply. Please include your CV along with the title of the position for which you are applying. Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans. Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law.

Coordinate and monitor shipments of patient and manufacturing materials ensuring compliance and timely delivery across the supply chain. | Experience in logistics coordination, knowledge of chain of custody, temperature-controlled shipments, and cross-functional communication in biotech or clinical trial environments. | Philadelphia, PA (Remote) Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on developing and launching targeted, potentially curative, cellular therapies for patients with autoimmune diseases. The CABA™ platform includes two strategies to treat and potentially cure many of the most common and challenging autoimmune diseases. The CARTA strategy, or Chimeric Antigen Receptor T cells for Autoimmunity, is designed to potentially reset the immune system by causing transient B cell depletion with early academic clinical data suggesting the potential of this strategy to transform treatment in patients with SLE and the possibility of cures in rheumatoid arthritis, myositis, and systemic sclerosis, among others. Our lead product candidate using the CARTA strategy is CABA-201, 4-1BB-containing CD19-CAR T designed specifically to treat patients with autoimmune diseases and which uses a CD-19 binder that has an encouraging clinical tolerability profile. The second strategy is Cabaletta Bio’s proprietary CAART, or chimeric autoantibody receptor T cells, strategy, which is designed to cause antigen-specific B cell depletion of well-defined, disease-causing B cells. Our lead product candidate developed using the CAART strategy is being evaluated in a clinical trial for patients with mucosal pemphigus vulgaris (mPV) and our second product candidate is expected to initiate a clinical trial later this year in muscle-specific tyrosine kinase (MuSK) myasthenia gravis. Cabaletta Bio’s headquarters are located in Philadelphia, PA. For more information, visit www.cabalettabio.com and follow us on LinkedIn and Twitter. Uniquely Differentiated. Rapid. Elegant. At Cabaletta, we are driven by the shared mission of developing cures, where a patients’ own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew. We’re proud to be a Great Place to Work-Certified™ company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Work® About The Position The Logistics Coordinator is responsible for the coordination, booking, tracking, and communication of all patient material, manufacturing material, and finished product shipments across the cell and gene therapy supply chain. This role serves as a central point of contact between treatment centers, manufacturing sites, couriers, depots, and internal stakeholders to ensure timely and compliant movement of critical patient-specific materials. The Logistics Coordinator proactively monitors shipments, manages transportation milestones, communicates status updates, and escalates risks to support uninterrupted patient treatment schedules. Responsibilities Shipment Coordination & Booking • Coordinate domestic and international transportation bookings for patient leukapheresis collections, starting materials, intermediates, and finished drug products. • Schedule and confirm shipments with approved specialty logistics providers and courier partners. • Ensure transportation arrangements align with manufacturing schedules, patient treatment dates, and chain of identity/chain of custody requirements. • Prepare and review shipping documentation, customs paperwork, and transportation instructions as required. • Verify shipment readiness and ensure all required packaging, labeling, and documentation are available prior to dispatch. Shipment Tracking & Monitoring • Monitor shipments from pickup through final delivery using transportation management systems and courier tracking platforms. • Provide proactive oversight of critical patient shipments to ensure adherence to planned timelines and temperature requirements. • Investigate transportation delays, route deviations, temperature excursions, and delivery issues. • Coordinate corrective actions with logistics providers and internal stakeholders to minimize patient impact. • Maintain accurate shipment records and tracking information in designated systems. Communication & Stakeholder Management • Serve as the primary communication point for shipment status updates across internal and external stakeholders. • Provide timely updates regarding shipment milestones, exceptions, and potential risks. • Coordinate communication between treatment centers, manufacturing facilities, couriers, quality teams, scheduling teams, and patient operations groups. • Facilitate escalation management for critical transportation events and ensure rapid stakeholder notification. • Participate in daily operational meetings and provide shipment status reports. Operational Excellence & Compliance • Ensure all logistics activities comply with GDP, GMP, GxP, IATA, DOT, and applicable regulatory requirements. • Maintain chain of identity and chain of custody documentation throughout the transportation process. • Support deviation investigations and root cause analysis related to shipment exceptions. • Contribute to SOP development, process improvements, and continuous improvement initiatives. • Monitor logistics performance metrics and assist in developing corrective and preventive actions. Preferred Qualifications • Experience in cell and gene therapy, biopharmaceutical, clinical trial, or healthcare logistics. • Knowledge of chain of custody and chain of identity requirements. • Familiarity with cryogenic and temperature-controlled transportation. • Experience managing international shipments and customs documentation. • Experience with transportation management systems (TMS) or logistics control toweroperations. Key Competencies • Attention to detail • Customer and patient focus • Sense of urgency • Problem solving and critical thinking • Cross-functional collaboration • Risk identification and escalation management • Time management and prioritization • Adaptability in a fast-paced environment Our name – Cabaletta – is derived from the operatic term for the second part of an aria that is designed to highlight the technical expertise of the lead singer. While our company is not the first to develop chimeric T cells as therapies, we are the first to develop them in a way that leverages T cells to specifically eliminate only B cells that cause disease, while sparing healthy B cells. Utilizing the backbone of this core technology, we expect to advance our portfolio with a rapid and repetitive rhythm, similar to the rhythm that is typical of a cabaletta. For more information, please visit https://www.cabalettabio.com/ or email careers@cabalettabio.com directly to apply. Please include your CV along with the title of the position for which you are applying. Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans. Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law.

Coordinate international logistics, trade compliance, and vendor management to support global supply chain operations. | Requires 3-6 years logistics or supply chain experience in pharma/biotech, international shipment management, and strong organizational and communication skills. | Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on developing and launching the first curative targeted cell therapies designed specifically for patients with autoimmune diseases. The CABA™ platform encompasses two complementary strategies which aim to advance the discovery and development of engineered T cell therapies with the potential to become deep and durable, perhaps curative, treatments for a broad range of autoimmune diseases. The lead CARTA (Chimeric Antigen Receptor T cells for Autoimmunity) strategy is prioritizing the development of rese-cel, a 4-1BB-containing fully human CD19-CAR T cell investigational therapy. Rese-cel is currently being evaluated in the RESET™ (REstoring SElf-Tolerance) clinical development program spanning multiple therapeutic areas, including rheumatology, neurology and dermatology. Cabaletta Bio’s headquarters and labs are located in Philadelphia, PA. For more information, please visit www.cabalettabio.com and connect with us on LinkedIn. Uniquely Differentiated. Rapid. Elegant. At Cabaletta, we are driven by the shared mission of developing cures, where a patients’ own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew. We’re proud to be a Great Place to Work-Certified™ company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Work® Title: Sr. Associate of Logistics / Supply Chain - International Location: Must be located in Switzerland or Germany and can work remotely About The Position The Logistics / Supply Chain Associate International plays a critical role in supporting Cabaletta’s global “vein-to-vein” supply chain operations, with a strong focus on international logistics execution, trade compliance support, and vendor coordination. This role acts as the operational extension of the International Supply Chain function, ensuring seamless execution of cross-border patient material movements, close coordination with logistics providers, and alignment of supply chain processes with evolving clinical and regulatory requirements. The position is ideally suited for someone who combines strong executional rigor with an interest in developing expertise in advanced therapy supply chains and international trade. Key Responsibilities International Logistics & Shipment Execution • Coordinate and oversee end-to-end international shipments (apheresis, drug product, intermediates). • Ensure full compliance with chain-of-identity (COI) and chain-of-custody (COC) requirements. • Prepare, review, and validate shipping and customs documentation (commercial invoices, HS codes, import/export documentation). • Act as primary operational point of contact for couriers, customs brokers, clinical sites, and manufacturing partners. • Monitor shipment status in real time and proactively manage risks, delays, and contingencies. Trade Compliance & Cross-Border Support • Support implementation and execution of international trade compliance processes. • Assist with HS code classification, country of origin determination, and Incoterm selection. • Support Importer/Exporter of Record (IOR/EOR) processes and documentation requirements. • Ensure audit-ready documentation and support inspections as required. • Identify and escalate potential compliance risks or deviations. Vendor & Partner Management Support • Coordinate operational interactions with logistics providers, CDMOs, and cryopreservation partners. • Track and report vendor performance (e.g. on-time delivery, deviations, responsiveness). • Support issue resolution and escalation management. • Assist in onboarding and qualification of new logistics vendors. Clinical Operations Support (Vein-to-Vein) • Support treatment center readiness by ensuring shipping lanes and documentation processes are in place. • Coordinate scheduling of patient-related shipments across stakeholders. • Ensure supply chain execution aligns with clinical timelines and patient needs. Process, Systems & Data Management • Maintain accurate and audit-ready records for shipment documentation, inventories, and vendor interactions. • Support development and continuous improvement of supply chain tools and tracking systems (e.g. ERP, visibility platforms). • Analyze logistics data to identify trends, risks, and improvement opportunities. Deviation & Risk Management • Support investigation of shipment deviations, temperature excursions, and documentation discrepancies. • Document and track CAPAs in collaboration with Quality teams. • Identify recurring issues and support implementation of mitigation plans. Qualifications Required • Bachelor’s degree in Supply Chain, Business, Life Sciences, or a related field; equivalent or relevant higher education will also be considered • 3–6 years of experience in logistics or supply chain within the pharmaceutical or biotechnology industry. • Experience managing international shipments and related documentation. • Strong organizational skills with high attention to detail. • Excellent communication skills across internal and external stakeholders. • Conversational proficiency in English and at least one additional EU language (e.g. German, French, Italian, or Spanish) Preferred • Experience in cell and gene therapy or advanced therapy supply chains. • Exposure to cryogenic (LN2 / ultra-low temperature) logistics. • Basic understanding of trade compliance concepts (HS codes, Incoterms, import/export processes). • Experience working with specialized 3PL providers (e.g. Cryoport, World Courier, Marken). • Experience supporting cross-border operations (EU, US, or global clinical supply chains). Personal Attributes • Highly detail-oriented with strong ownership mindset. • Able to operate independently in a fast-paced and high-stakes environment. • Strong problem-solving skills with proactive risk management approach. • Collaborative team player with ability to align cross-functional stakeholders. Our name – Cabaletta – is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression. For more information, please visit https://www.cabalettabio.com/join-our-crew Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans. Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation. And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm.