1.Develop and optimize analytical methods for characterization of biotherapeutics in pre-clinical and clinical stages.
2.Write Standard Operation Procedure (SOP)
3.Develop analytical methods for intermediates as part of PAT (Process Analytical Technology)
4.Involved in analytical method transfer from other companies.
5.Perform all experiments under applicable safety and regulatory compliances.
6.Generate high quality results in support of analytical testing of growing drug pipeline.
7.Document data/results according to applicable compliances, such as GMP.
8.Effective communication of data/results through written documentation and oral presentations.
9.Accountable for completing the assigned tasks and communicate results in a timely manner.
10.Accountable for completing the assigned tasks and communicate results in a timely manner.
1.A master degree with 5+ years or a Ph.D. with 2+ years of experience in analytical science or equivalent within a biopharmaceutical industry.
2.Strong hands-on experience in HPLC (SEC, IEX, RP), LC-MS (peptide mapping and N-linked glycan) and CE (cIEF and CE-SDS).
3.Ability to work independently and to manage multiple projects at one time.
4.Ability to work independently and to manage multiple projects at one time.
5.Eager and quick to learn, self-driven and motivated.