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Senior Research Associate Job

Read the Senior Research Associate (job description) to understand the position requirements.



    The successful applicant will have a working understanding of downstream process development scale up including centrifugation, normal flow filtration, chromatography operations, tangential flow filtration virus inactivation/removal. The ability to demonstrate a significant level of hands on experience in several of these areas is expected.
    The applicant is expected to work effectively within the purification team to help design execute experiments supporting process definition, optimization, characterization process transfer activities with an increasing level of independence.
    The applicant will collaborate with Technical Operations in technology transfer from process development to clinical commercial GMP manufacturing, including definition of bill of materials, batch record drafting/review discrepancy resolution. Serves as process development representative during purification operations, provides technical trouble-shooting identifies opportunities for future process equipment improvements. The applicant will also contribute to the preparation of regulatory filings process validation characterization reports.
    The applicant should be an effective communicator of ideas, project goals results to the team should have the ability to proactively identify issues suggest solutions in a collaborative multidisciplinary environment. This is a highly collaborative environment where willingness ability to communicate work effectively with individuals across various teams is essential.
    Candidates should be self-motivated, organized enjoy scientific investigation thinking. The applicant is also expected to recommend alternatives, research new methods technologies that can advance purification platforms proactively seek out senior personnel to discuss potential solutions to problems. The applicant will monitor contribute to external literature scientific conferences. Plans executes assigned experiments that support Process Development activities project goals.
    Requires a BS (5 years of experience) or MS (3 years) in Chemical/Biochemical Engineering, Biochemistry or a related scientific discipline of relevant experience that demonstrates expertise in purification process development sustained excellence in performance accomplishments that align with company goals.
    Hands-on execution of all aspects of purification process development, process scale up GMP manufacturing support. Works with increasing level of independence in the initiation execution of laboratory experimentation while proactively seeking out senior personnel to define goals, design experiments, discuss results suggest next steps.
    About Kelly Services .
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