Bioanalytical Scientist
 Position Summary:​​

The new hire will:
  • The candidate should possess deep scientific and technical knowledge and experience in developing, transferring, optimizing and validating assays to support pre-clinical and clinical development of Cello’s nanoparticle technology.
  • Be responsible for development and implementation of bioanalytical assays using appropriate fit-for-purpose assay technologies to support nonclinical, clinical product development.
  • Work with CROs to support GLP pre-clinical studies such as PK and TK, serve as technical expert on assay trouble shooting, and assist in review of assay qualification/validation reports and sample analysis reports from CROs.
  • Write bioanalytical method protocols, sample analysis procedures, and reports.
  • Be responsible for data QC and bioanalytical reports.

  • Extensive academic and industry experiences in development and assessment of GLP bioanalytical assays related to protein markers on cell surface.
  • Life science degree required – PhD with 2+ years of working experience.
  • Technical expertise in bioanalytical assay development, optimization, and validation for biologics. Hands-on experience with assay development is required.
  • Experience in managing outsourced bioanalytical activities at CROs, or experience in working within a CRO.
  • Experience in working in a regulated environment.
  • Strong organizational skills with attention to details, budget, and timelines.
  • Excellent verbal and written communication skills including technical writing skills.
  • Ability to thrive in a highly collaborative, fast-paced, and team-oriented environment.  

Successful candidate must be authorized to work in the United States.
Cello Therapeutics, Inc. is an equal opportunity employer.

Please submit a resume/CV to [email protected] if interested.