Process Development Senior Associate

Target PR Range: 19-26/hr DOE 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 scienceWorking 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 #J-18808-Ljbffr Planet Pharma