Cell Therapy Jobs

Lead operational execution for Medical Affairs at BlueRock by managing cross-functional projects, vendor relationships, budgets, and medical conference and RWE logistics to advance clinical-stage cell therapy programs.

Lead and execute global medical and scientific communications for BlueRock's neurology and ophthalmology cell therapy programs, ensuring high-quality, compliant publications, congress strategy, and KOL engagement.

Bristol Myers Squibb is hiring a Manager of Operational Excellence at its Devens cell therapy site to drive lean transformation, capacity modeling, and measurable process improvements across operations and supply chain.

Vertex is hiring a hybrid contract Project Manager with CDMO and tech-transfer experience to lead cross-functional CMC projects supporting cell and gene therapy development.

Experienced analytical science SME needed to lead development, validation, and network implementation of rapid microbiology safety methods for Vertex’s biologics and cell & gene therapy commercial programs on a 24-month part-time contract.

Lead the Analytical Technologies effort within BMS Cell Therapy Analytical Development to streamline assay workflows, implement automation, and speed product development.

Cellares is hiring a Senior Director, IDMO Site Quality to lead QA and QC for its Bridgewater cGMP cell therapy manufacturing site, driving quality systems, regulatory compliance, and team development.

Lead the Material Review Board at BMS Devens to evaluate non-conforming cell therapy material, coordinate cross-functional risk assessments, and deliver disposition options that enable safe patient treatment.

Bristol Myers Squibb seeks a Specialist, Investigations to lead deviation investigations and CAPA activities within its cGMP cell therapy manufacturing site in Devens, MA.

Orca Bio is hiring a 2nd-shift Supervisor, Clinical Manufacturing to oversee on-site cell therapy production in Sacramento, ensuring quality, compliance, and efficient shift operations.

Bristol Myers Squibb is hiring a Senior Engineer for IT Computer System Validation at the Devens Cell Therapy Facility to lead CSV lifecycle activities, act as a CSV SME, and ensure computerized systems meet GxP and regulatory standards.

Technical Writer needed to author and manage CMC regulatory submission content (eCTD/CTD) for a cell therapy portfolio in a hybrid, cross-functional PMO role supporting a biopharma client.

Vertex is seeking a Senior QA Specialist (2nd shift, contract) to drive GMP-compliant product disposition and on‑floor quality oversight for cell and gene therapy drug product operations.

Lead late-phase process development and bioreactor-based stem cell process optimization for Vertex's cell and gene therapy programs at the Boston Seaport site in a temporary, hands-on lab role.

Lead the digital manufacturing strategy and operational technology programs at ElevateBio to modernize MES/LIMS/automation platforms and enable scalable, compliant cell and gene therapy manufacturing.

The Abramson Cancer Center is hiring a Clinical Research Coordinator B/C to coordinate complex oncology clinical trials within the Cell Therapy & Transplant Research Team at Penn Medicine.

Experienced project manager needed to lead cross-functional CAR T manufacturing projects and tech transfers within a hybrid site environment at Bristol Myers Squibb.

Experienced operations leader sought to lead business planning, budgeting, and cross-functional delivery for AstraZeneca's Immunology Cell Therapy organization.

Lead and scale Orca Bio’s scientific communications and publications strategy to support Medical Affairs, MSL engagement, congress execution, and preparation for commercial launch.

Senior leader sought to define and execute global oncology market access, pricing and HEOR strategy across launched and pipeline assets for Bristol Myers Squibb from the Princeton hub.

Lead Orchard’s US regulatory science strategy as Executive Director, advising cross-functional teams and managing FDA interactions to advance the company’s pipeline.

Northwestern Medicine seeks a Senior Regulatory Coordinator to lead IRB submissions and regulatory oversight for complex stem cell transplant and cell therapy studies within the Autoimmune Diseases program.

Clinical Research Coordinator A/B needed at Penn's CCI to support coordination, documentation, and regulatory compliance for early-phase oncology cell and gene therapy trials.

Experienced QA professional needed to lead GMP quality oversight, batch disposition, and investigations for drug product operations at a client site supporting clinical and commercial manufacturing.

Experienced microbiology QC scientist needed to perform sterility and environmental monitoring testing and implement contamination control strategies at Orca Bio’s Sacramento manufacturing site.

University of Chicago Medicine is hiring a dedicated Staff Nurse (RN) for the 10E Oncology/SCT night team to deliver advanced, compassionate care for complex cancer and transplant patients.

Novartis is hiring a Senior Expert in Process Analytics to lead analytical method development and assay troubleshooting for gene and cell therapy programs at the Durham site.