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Cabaletta Bio Inc

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Supply Chain Associate

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Join Cabaletta Bio in Philadelphia as a Supply Chain Associate. Support end-to-end clinical cell therapy operations, managing critical shipments and raw materials. This role requires a bachelor's degree or 3-5 years' experience, strong organizational skills, and a collaborative mindset. Enjoy a f...
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United States , Philadelphia
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Not provided
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Until further notice

Vice President, Market Access, Commercial

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Lead market access strategy for innovative autoimmune CAR-T therapies in Philadelphia. This senior role requires 15+ years of biopharma experience, specializing in cell/gene therapy and payer negotiations. You will secure optimal coverage and reimbursement, shaping patient access. We offer compet...
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United States , Philadelphia
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Not provided
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Talent Acquisition Specialist

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Join Cabaletta Bio as our sole full-cycle Talent Acquisition Specialist in Philadelphia. You will drive recruitment, from sourcing to offers, using tools like LinkedIn Recruiter and our ATS. Partner with hiring managers to build our team and refine scalable processes. Enjoy health benefits, retir...
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Location
United States , Philadelphia
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Not provided
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Until further notice

Process Engineer, Manufacturing Science & Technology

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Join our MSAT team in Philadelphia as a Process Engineer for cell therapy commercialization. You will drive process optimization, tech transfer, and characterization to ensure robust, scalable manufacturing. The role requires experience in cGMP biologics, late-stage activities, and BLA-enabling d...
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Location
United States , Philadelphia
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Not provided
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Audit Director, Quality & Compliance

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Lead our GxP audit program as an Audit Director in Philadelphia. You will develop strategy, oversee internal/external audits, and ensure compliance with global regulations (FDA, EMA). Mentor a team and drive quality in a fast-paced cell therapy environment. Competitive benefits include health, re...
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Location
United States , Philadelphia
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Not provided
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GMP QC Specialist, CMC

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Join our Philadelphia team as a GMP QC Specialist, CMC. Ensure GMP compliance for internal and external QC data in a biopharmaceutical setting. Utilize your 5+ years of experience in QC/quality operations and expertise in cell/gene therapy assays. Enjoy health benefits, retirement plans, PTO, and...
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Location
United States , Philadelphia
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Not provided
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Vice President and Head of Information Technology

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Lead IT strategy and infrastructure for a biotech leader in Philadelphia. This executive role requires 10+ years of leadership, with deep expertise in GxP, cloud platforms, and cell therapy commercialization. Build and scale secure, compliant systems while enjoying competitive health, retirement,...
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Location
United States , Philadelphia
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Sr. Director, Clinical Scientist

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Lead the clinical science strategy for groundbreaking CAR-T cell therapies in autoimmune diseases. This senior role in Philadelphia requires deep expertise in clinical development, T-cell biology, and autoimmune disorders. You will drive trials from concept to BLA submission, ensuring scientific ...
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United States , Philadelphia
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Not provided
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Manager, Clinical Operations, International

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Lead international clinical trials for innovative cell therapies in Germany or Switzerland. This role requires 4+ years of trial management experience, including CRO oversight and knowledge of European regulations. You will ensure quality and compliance from study start-up through close-out, with...
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Germany; Switzerland
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Senior Medical Director, Clinical Development

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Lead clinical development for innovative cell therapies in autoimmune diseases at Cabaletta Bio. This hands-on Senior Medical Director role in Philadelphia requires an MD/PhD with 7+ years in biotech/pharma clinical trials. Provide medical oversight from early to late-stage studies, collaborating...
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United States , Philadelphia
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Associate Director, Regulatory

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Lead regulatory strategy for a pivotal cell therapy program from clinical trials to BLA/MAA submission. Utilize your 5+ years of biopharma regulatory experience, including direct BLA expertise, to guide cross-functional teams and engage with global health authorities. This Philadelphia-based role...
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Location
United States , Philadelphia
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Not provided
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Senior Director, Clinical and Regulatory Writing

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Lead the clinical writing strategy for innovative cell and gene therapies in Philadelphia. This senior director role requires 12+ years of regulatory writing experience, including BLAs/MAAs, and strong leadership skills. You will oversee high-quality submissions and mentor a team, supported by co...
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Location
United States , Philadelphia
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Salary
Not provided
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Until further notice