NOTE: PLEASE SUBMIT BOTH RESUME AND COVER LETTER TO APPLY FOR THIS JOB. KINDLY DISCUSS YOUR MOTIVATION, RELEVANT EXPERIENCE, SALARY REQUIREMENTS, AND VISA STATUS IN YOUR SUBMISSION.
Job Duties
- Complete Immunoassay Development, Troubleshooting, Optimization, or Immunoassay Transfer of customized, robust, and highly sensitive methods for quantitating large molecules, biologics, cytokines, peptides, etc.
- Deliver GLP and non-GLP ELISA, Mesoscale Discovery (MSD) ECL, qPCR, and Luminex Multiplex Analysis for Pharmacokinetic (PK), Toxicology (Tox), Biomarker, Bioavailability (BA), Biosimilar, Immunogenicity (ADA, nAB), and other bioanalytical studies
- Perform fit-for-purpose Ligand Binding Assay (LBA) Method Validation, stability testing, and high-quality bioanalytical sample analysis as per FDA/ICH/EMA guidelines
- Carry out challenging method development, troubleshooting, optimization, and validation processes; plan independently the entire set of initial runs, carefully review data (overall signal, titration, signal-to-noise, matrix interference, recovery, CV, etc.), fine tune assay parameters, and iterate as frequently as needed for a robust and reproducible GLP validation ready method
- Prepare timely documentation and reports covering objectives, methods, analysis, and results for drug and biomarker bioanalysis in a variety of species and biological matrices (whole blood/plasma/serum, urine, tissue homogenate, etc.)
- Troubleshoot complex assay, identify kit/material issues (ELISA, Mesoscale Discovery ECL, and Luminex Multiplex), and resolve with vendors
- Follow Good Laboratory Practices (GLP), Company Standard Operating Procedures (SOPs), and Sponsor Study protocols
- Train and mentor team members on laboratory procedures, instrumentation, software, and equipment
If interested, please e-mail your resume to careers@nebiolab.com.