The position requires analyst participation in development and qualification of diagnostic ligand-binding assays for candidate and post-market vaccines in support of various programs.
Responsibilities:
·Generation and characterization of reagents, performance of experiments for development and qualification of assays, assay throughput for the pre-clinical studies and writing related procedures and reports.
·As an integral member of the dynamic team, the incumbent must have a strong work ethic and be highly collaborative with the other group members.
·All of the above includes practicing laboratory safety at all times and efforts toward GLP compliance.
·Perform all aspects of to support assay development and clinical testing.
·Provide critical data review of clinical and non-clinical data. Collect, collate and analyze data on a per project basis to support troubleshooting, qualification and other lab projects.
·Perform assays to support critical assay reagent testing, assay development/ troubleshooting.
·Assist in ordering supplies from internal inventory and order/prepare reagents/supplies necessary for assay work.
·Assist in updating and writing documents associated with assays, including information/data archiving, SOPs and status reports.
·Satisfactorily completes all GLP and safety training in conformance with Departmental requirements.
·Attend Power2Learn, corporate, and departmental training, as available.
·Must meet Vaccine Research Medical Surveillance requirements