Sr Associate

Note:
Fully Onsite
Working Schedule: Dayshift 8 - 5PM
Process Development Senior Associate
What you will do
Let s do this. Let s change the world. In this vital role you will work in collaborative matrix environment including partner functional areas to support product and process characterization studies, data analysis and investigations.
Analyze late stage protein pharmaceutical products with advanced analytical methods including capillary electrophoresis, chromatography and mass spectrometry techniques to support product and process characterization in a cross-functional team environment to advance therapies
Lead or contribute to development, optimization and troubleshooting of analytical methods, participate in qualification, transfer and validation experiments with a focus on separation-based purity methods
Independently prioritize, manage, and schedule multiple tasks including: data analyses, maintenance of electronic notebook records of experimental data, participation in authoring of technical protocols and reports, and presentation of results in internal meetings in order to meet deliverables
Basic Qualifications
Master s degree or Master's by time of hire
Bachelor s degree and 2 years of scientific / pharmaceutical experience
Associate s degree and 4 years of scientific / pharmaceutical experience OR
High school diploma / GED and 6 years of scientific / pharmaceutical experience
Preferred Qualifications
Degree in chemistry, biochemistry, biophysics, pharmaceutical sciences, or related discipline.
Excellent laboratory skills
Hands on laboratory experience with liquid chromatography and capillary electrophoresis (e.g. HIC, SEC, IEX, RP, HILIC, CE-SDS, and cIEF/icIEF,), including instrument handling and troubleshooting
Experience with CE and LC analysis software
Hands on experience with method qualification and transfer
Strong desire to learn and interest in science
Working knowledge of data processing and analysis tools in Excel and other statistical software
Understanding of phase-appropriate GMP compliance and documentation
Well-organized; ability to multitask, effectively plan and follow through on complex projects, and to work both independently and in teams