Description:
\t\t\t\t\tPosition SummaryThe Associate Scientist II is part of a team responsible for development of stable formulations, drug delivery systems, and manufacturing processes for recombinant adeno-associated virus (AAV) gene delivery products. In this role you will contribute to formulation development, characterization, and stability studies; design of drug product presentations; process development; clinical compatibility studies; and aseptic fills for GLP studies for multiple projects. You will work both independently and as a part of cross-functional teams on assigned projects, prioritize projects to meet departmental and organizational goals, and communicate results in technical reports and presentations. Essential Position Requirements \tContribute to individual formulation development, characterization, compatibility, and stability studies\tContribute towards individual drug product process design, characterization studies, and aseptic fills for GLP studies\tContribute to pertinent regulatory submission sections including INDs, BLAs, and equivalent\tPerform relevant methods and techniques in support of pharmaceutical development goals
\t\t\t\t\tSkills:
\t\t\t\t\tFormulation, Chemistry, Formulation Development, Characterization, Compatibility, Stability, GLP, Product Process Design, Bioanalytical, Dynamic light scattering, spectrophotometry, HPLC
\t\t\t\t\tTop Skills Details:
\t\t\t\t\tFormulation,Chemistry,Formulation Development,Characterization,Compatibility,Stability,GLP,Product Process Design,Bioanalytical,Dynamic light scattering,spectrophotometry,HPLC
\t\t\t\t\tAdditional Skills & Qualifications:
\t\t\t\t\tExperience and Qualifications\tBachelor’s degree in relevant scientific discipline with at least 2+ years relevant industry experience or Master’s degree in relevant scientific discipline with 1+ year of relevant industry experience\tFamiliarity with theoretical and practical knowledge of formulation development and characterization principles\tIdeally has an understanding of aseptic fill-finish of biologics, including unit operations, GMP requirements, media simulations, container/closure integrity, and regulatory requirements\tIdeally has an understanding of bioanalytical techniques for product characterization and product stability evaluation, including dynamic light scattering, spectrophotometry, subvisible particle analysis, and HPLC\tAble to locate relevant scientific literature and standard industry guidance documents\tAbility to perform routine data analysis\tAbility to perform experiments that support scientific activities and project goals\tAbility to interpret data and draw conclusions.\tAbility to effectively communicate information and results in the appropriate format (i.e. lab notebooks, presentations, etc.)\tMust be able to work collaboratively and effectively as part of a team\tPrior industry experience preferred
\t\t\t\t\tExperience Level:
\t\t\t\t\tIntermediate Level
About ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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