Carisma Therapeutics Inc. seeks Process Development Scientist for downstream, to lead experimental design, planning and execution of viral vector purification laboratory studies for development, optimization and manufacturing of macrophage and antigen-presenting functions to attack cancers. Duties include design, execute and support analytic methods for process development studies and collect, analyze data to present findings to business stakeholders, author and review protocols, technical reports, regulatory source documents and memos to summarize experiments and investigations and participate in a cross-functional team meetings to transfer technology to cGMP manufacturing partners.
Requirements: Masters in Chemical or Biomedical Engineering and two years’ experience as a process or downstream scientist in research and development in biopharmaceutical industry or laboratory setting; working with Tangential Flow Filtration (TFF), UF/DF, Chromatography, and downstream unit operations; design and executing experiments and optimizing purification process; design and execution of development studies to identify and determine process parameter ranges for purification process steps; maintaining Electronic Lab Notebooks (ELN) with GMP standards; and ability to analyze, interpret, and act on data generated during experiments using JMP or other analytical software. Location: 3675 Market Street, Fl.
6, Philadelphia, PA 19104.Carisma Therapeutics is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.Carisma Therapeutics is proud to be a 2021 Best Places to Work Honoree.Apply for this job
