Key responsibilities

• You’ll develop and qualify highly sensitive, reliable LCMS methods for the rapid and accurate analysis of biologic, viral vector, and RNA modalities.
• You’ll perform in-depth mass-spec and biophysical characterization using state-of-the-art equipment.
• You’ll identify emerging practices and drive scientifically innovative method development.
• You’ll troubleshoot assays and apply design of experiments (DOE) and other systematic and statistical approaches to method development, as needed.
• You’ll help grow, mentor, and provide scientific expertise to the analytical sciences team.
• You’ll represent the analytical sciences team on cross-functional projects and effectively communicate results, progress and plans.
• You will be comfortable working within an evolving hybrid team structure at our brand new labs in Boston’s Fenway neighborhood.

Qualifications

• You’re a creative problem solver and get excited about the opportunity to drive the creation of industry-disruptive technology.
• Developing and executing LCMS assays of biologic therapeutics is squarely in your wheelhouse, stemming from years of experience. 
• You have experience performing HPLC/UPLC analysis of biologics or viral vector therapeutics.  
• You have a Ph.D. in Biochemistry, Chemistry, Biological Engineering, or a related field.
• You have 3+ years of hands-on industry experience performing mass-spec and biophysical characterization in support of biologic therapies.
• Don’t let this stop you from applying, but it’s a plus if you are experienced at running GXII, cSDS, CE-SDS or equivalent methods.   
• Experience utilizing statistical tools such as ANOVA analysis, Design of experiment (DOE) is preferred.
• Experience working with a global customer base isn’t a requirement for this role but bonus points if you have it. 
• You work best as an individual contributor working within a team to drive projects forward.