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    PH

    Phil Ellis Associates, Inc.

    Engineering Consulting

    Bioprocess Engineer

    Huntsville, United StatesOn-SiteFull-time4+ yrs experiencePosted 3w ago
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    Job description

    Company is seeking to hire a Bioprocess Engineer to support the company’s ongoing development of novel immunotherapies. The position will play an integral role in the establishment of a GMP manufacturing facility to produce plasmid DNA active pharmaceutical ingredient (API).

    ·       Lead the development of pilot scale downstream processing (DSP) unit operations of plasmid DNA from bacterial cell paste (from 10 L - 100 L bioreactor fermentation), to include lysis, clarification, ultrafiltration/diafiltration, and ion exchange chromatography.

    ·       Plan and execute structured process development experiments to achieve the target yield, process optimization, product quality, scale-up and process robustness objectives.

    ·       Play a pivotal role in the establishment of a GMP manufacturing facility to produce plasmid DNA active pharmaceutical ingredient (API).

    ·       Document work thoroughly with a detail-oriented approach, write concise technical reports, and make effective presentations to management and other team members.

    ·       Translate developed processes into standard operating procedures (SOPs) as well as necessary calibration and preventive maintenance SOPs.

    ·       Write validation protocols and lead the technical support staff to successfully execute IQ, OQ, and PQ.

    ·       Lead the process transition into the new facility.

    ·       Troubleshoot, optimize, and improve ongoing process activity with scientific curiosity.

    ·       B.S. or M.S. degree in Biochemical/Chemical Engineering preferred. Will also consider other disciplines such as biology, chemistry, or related field with requisite experience.

    ·       4+ years of hands-on biopharmaceutical experience at pilot or commercial scale with bioreactor fermentation (USP) and DSP of plasmid DNA from bacterial cell paste, including lysis, clarification, ultrafiltration/diafiltration, and ion exchange chromatography.

    ·       2+ years of experience working in a GMP manufacturing environment. Candidates with supervisory experience are preferred.

    ·       Significant experience using ultrafiltration and diafiltration with tangential flow filtration (TFF) in a DSP unit operation.

    Competitive salary, bonus, stock, relocation and benefits are offered.

    Job details are sourced from the employer's original posting.

    Open job posting
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    About the company

    Phil Ellis Associates, Inc.

    A rapidly growing international engineering/project management, long-term consulting firm

    View all Phil Ellis Associates, Inc. jobs
    Industry
    Engineering Consulting
    Open roles
    3

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