Goodall Brazier are partnered with an exciting CDMO, specializing in the manufacturing of peptides, oligonucleotides and related compounds.
This position will be based in Los Angeles, California and looking to develop, implement and maintain all aspects of the Oligonucleotide Program.
Primary responsibilities: .Analysis of chemically synthesized oligonucleotide: LC-MS, UV-Vis, IEX, and RP-HPLC.
Purity evaluation and sequence determination of oligonucleotides based on analytical data Development / Tweaking of test methods Experience in duplex denaturing and non-denaturing HPLC methods Present results clearly in both written and oral format Knowledge of qualification/validation of analytical test methods Closely partner with QA and QC peers Write development reports and present results internally and externally Other duties as assigned Position requirements: Minimum MS in chemistry with a concentration in analytical chemistry Minimum experience 2-5 years in an API GMP manufacturing facility Strong knowledge of oligonucleotide analytical techniques Technical writing Excellent communication skills are a must CDMO experience is a plus Salary: $95-180k (DOE)