Scientist, Analytical Development

Scientist, Analytical Development
Boston, MA

Our client is a pre-clinical, VC-backed biotechnology company that is leveraging naturally derived extracellular vesicles (EVs) to deliver gene therapies in vivo. They are operating on a hybrid-virtual model. Meetings are mostly virtual, but teams will meet in person to whiteboard strategy, visit partners to advance programs, and celebrate wins!


The Analytical Development Scientist position is full-time and will be 100% in-person designing and conducting experiments. You will work directly with the CMC leadership at the client and its CDMO partner to manage process development, optimization, process scale-up, and preclinical manufacturing. This is a critical development position that enables working in cross-functional teams, learning and developing all aspects of manufacturing process (upstream, downstream, and analytics) and provides significant career growth opportunities.

To be successful in this role, you should be someone who is self-starter, always up or a challenge and finds the unique demands of the fast-paced startup environment motivating. You will need to be adept at managing both internal projects and external collaborations, and be able to do both while espousing the people-first, simplicity-oriented values we hold as core to culture.


  • Independently develop, execute, and document analytical method development and qualification in support of process development, product release and stability, and product characterization of Extracellular Vesicles (EV)
  • Act as a SME for Analytical Development and responsible for knowledge/technology transfer of in-process and product characterization methods to partners
  • Author and review SOPs, technical reports, and supporting procedures for analytical development.
  • Maintain, calibrate and operate analytical equipment and instruments
  • Work closely with team members (internal and external) to maintain project development, implementation and troubleshooting of experiments, and ensure deliverables for both internal research projects and external scientific partnerships
  • Attend and present at team meetings to share results, and plan projects and experiments, with a keen eye for achieving company milestones
  • Perform other duties as assigned, including all those associated with facilitating the smooth operation in the lab.


  • PhD in biology, biomedical science, immunology, pharmaceutical science or related field with 1+ years relevant experience, MS degree with 5+ years relevant experience or BS with 8+ years relevant experience
  • Analytical and Problem-Solving Skills – Able to troubleshoot critical issues or problems and determine causes and possible solutions.
  • Ability to balance/prioritize research efforts across multiple programs, meet deadlines, and shift plans in service of a rapidly changing startup environment
  • Attention to detail and the ability to work individually, within a multi-disciplinary team in a matrix environment, as well as with external partners and vendors.
  • Hands-on, roll-up-your-sleeves approach with high sense of urgency and drive for results
  • Proficiency with Microsoft Office suite, with excellent PowerPoint and Excel skills
  • Exceptional communication, writing, organizational and time management skills
  • Exemplary lab notebook practices, and attention to detail in recordkeeping


  • Knowledge and experience in developing and qualifying analytical methods for biologics or gene therapy products are highly preferred
  • Understanding of gene therapy vector characteristics and critical attributes so as to direct bioprocess development and product/process control strategies
  • Understanding of various cell and gene therapies, and gene editing technologies
  • Experience working with collaborators and CDMOs
  • Experience with electronic lab notebooks (ELNs)


  • Full-time Position
  • Salary and benefits consistent with the competitive market of Boston/Cambridge and commensurate with experience
  • In-person benchwork in Boston/Cambridge area and/or at partner headquarters location(s)
  • Current U.S. work authorization required