Scientist, Process Development

Responsibilities Design and execute process development experimental plans, author associated protocols and reports, and present data and insights to cross-functional teams. Develop phase-appropriate cell therapy manufacturing processes using Quality by Design (QbD) principles. Support technology transfer of processes to CDMOs for early-phase cGMP clinical manufacturing, as needed. Contribute to the development of platform manufacturing processes and ensure readiness for clinical and future commercial manufacturing. Identify and evaluate opportunities to improve manufacturing performance, including cost, throughput, robustness, and quality. Maintain laboratory materials and sample inventory to support experimental planning and execution. Accurately document experimental data in a timely manner, ensuring data integrity, traceability, and compliance with protocols. Maintain individual training

requirements in a compliant state. Contribute to regulatory filings (e.g., IND/CTA) and technical documentation, as needed. Other related duties, as assigned

Qualifications: Bachelors Degree with 4 + years experience or Masters Degree with 2 + years’ experience within biologics process development and manufacturing under cGMP processes. Experience with cell therapy manufacturing scale up, technology transfer, and process development methods, scale-up, and tech transfer methods is required. Experience of basic biological laboratory techniques such as cell culture, PCR, cell-based bioassays, and/or ELISA. Extensive flow cytometry experience is required.in flow cytometry and cell-based assays. Strong problem-solving skill is preferred. Experience supporting documents for regulatory review including but not limited to INDs, CTAs, and BLAs. Previous experience and working knowledge of T-cells or immunological cell therapies. Good working knowledge in cGMP manufacturing of biological process and ICH regulations. Highly organized and efficient, with a curiosity to be part of cutting-edge science. Strong team orientation and passion for continuous self-development. Ability to coordinate parallel tasks across multiple projects, demonstrating prioritization. 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. #LI-ONSITE Apply for this job First name Last name Email address Location Phone number Resume Attach resume Attach another file Attach file Add another What is your Linkedin Profile URL? Attach your Cover Letter - or: Attach Cover Letter Cut and Paste your Cover Letter below: What are your salary

requirements? Are you willing to relocate? Yes No Are you authorized to work in the United States? Yes No Will you now or in the future require sponsorship for employment visa status (e.g. H-1B status)? Yes No Linkedin url Should be {http://www.linkedin.com/pub/[member-name/]x/y/z} or {http://www.linkedin.com/in/string} © 2014-2026 TriNet Group, Inc. All rights reserved. Privacy Policy

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