 Test mRNA, LNP or DNA samples from pipeline discovery, platform research or CMC process development and issue internal reports based on established written procedures.  Develop new methods or optimize existing methods for specific purposes with the guidance from experienced colleagues.  Complete experimental records in a timely and accurate manner.  Draft technical documents as needed for internal reference or technical transfer.  Participate or present data in project-related meetings.  Any related lab operation work, e.g. instrument maintenance, sample and material management, etc.

 Master or bachelor’s degree in biology, chemistry or pharmaceutical-related disciplines.  ≥3 year’s (for master) or 5 years’ (for bachelor) experience in analytical development or QC of any biological drugs, e.g. antibody-based therapeutics or cellular and gene therapy products.  Extensive hands-on experience with at least one of the following techniques: cell-based assays, flow cytometry, ELISA, immunoblotting, etc.  Attention to details and record keeping.  Plus to have: experience with qPCR, mRNA-LNP products and/or IND projects; fluency in English reading and writing; effective communication.