Cello Therapeutics, Inc. is a rapidly growing biotech company
located in the Sorrento Valley—one of the major biotech hubs in the nation. Cello
focuses on the development of novel nanotherapeutics based on biomimetic cell
membrane-coated nanoparticles for cancer treatment. Cello offers a highly
motivational and rewarding working environment with attractive salary and
The candidate will 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.
Responsible for development and implementation
of bioanalytical assay 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 bioanalysis method protocols, sample
analysis procedures, and reports
Responsible for data QC and bioanalytical
Position is Full Time. Compensation: $80,000 to $120,000
Extensive industry experience in development
and assessment of GLP bioanalytical assays related to protein markers on cell
Life science degree required – PhD with 2+
years of experience.
Technical expertise in bioanalytical assay
development, optimization, and validation for biologics. Hands-on experience
with assay development is required.
Experience managing outsourced bioanalytical
activities at CROs, or experience working within a CRO.
Experience 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, team-oriented environment
Successful candidate must be authorized to work in the