Vacancy expired!
- Successfully execute advanced analytical studies on complex biologics using high performance LC-MS based platforms and related sample preparation approaches
- Collaborate with internal & external scientific teams in study execution and delivery
- Generate project data and results to enable successful delivery of project plans, milestones and timelines
- Participate in the development of analytic data and methods for regulatory packages in biologic drug development
- Prepare, review and present project progress, results and analysis both internally and externally
- Document experiments, results and findings in laboratory notebook and LIMS system
- Must be able to lead MS execution of experiments independently
- BS/MS or PhD degree in analytical chemistry with 1-3 years of biopharmaceutical or related CRO industry experience; Title will be commensurate with experience level
- The ideal candidate should have direct experience in analytical development in the field of biologics, gene therapies and/or vaccines
- Hands-on experience and in-depth understanding of protein characterization using LC-MS (e.g., Thermo QE series, etc.) and associated bioinformatics (e.g., BioPharma Finder, etc.) is required.
- Familiarity with LC-MS analysis of nucleic acid is a plus
- Familiarity with additional chromatographic (e.g., SEC, IEX) and/or electrophoretic (e.g., CE-SDS) approaches is a plus
- A strong background in bioanalytical chemistry, proteomics, assay development, in-depth protein and/or glycan characterization, including product and process related impurities identification and quantitation
- Experience with analytical method qualification, transfer, validation and general understanding of regulatory requirement (cGMP) for biotherapeutics development is a plus
- Enthusiasm for scientific excellence with motivation for making contributions in a team environment
- We hire for attitude and train for task!
Vacancy expired!