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Execute routine analytical tests and quality control assays, such as qPCR, ELISA, SDS-PAGE, Western blot, and HPLC, to assess the purity, potency, and safety of AAV vector products. Experience with molecular biology, biochemistry, or cell biology techniques and analytical methods (e.g., qPCR, Elisa, Western Blot.
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Experience in basic biochemistry laboratory techniques such as qRT-PCR, SDS-PAGE, Western blot, ELISA, etc. The RA I is expected to work closely with the Upstream Process Development, Downstream Process Development, Analytical Development and Vector Core groups to foster a collaborative environment delivering sound and robust manufacturing processes for AAV vectors.
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Expertise in lab techniques including, but not limited to, immunofluorescence, western blotting, ELISA, qPCR, qRT-PCR, flow cytometry, protein biochemistry, glycobiology, etc. Expertise in lab techniques including, but not limited to, immunofluorescence, western blotting, ELISA, qPCR, qRT-PCR, flow cytometry, protein biochemistry, glycobiology, etc.
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Strong experience managing external manufacturing operations at CMO's/CRO's/CDMO's in relation to bioassays such as ADCC, CDC, ELISA, SPR (Crucial), and Cell-based binding assays. Provide oversight and expertise for external manufacturing operations relating to bioassays such as ADCC, CDC, ELISA, SPR (Crucial), and Cell-based binding assays.
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