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Experience with technologies focused on mRNA drug substance process such as In-vitro transcription reactions, Enzyme based process and purification of biomolecules such as, Enzymatic reactions, AKTA, UF/DF, Column Chromatography.
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The successful candidate will have hands-on experience with cell-based in-vitro potency assays, SDS-PAGE, Automated Western blot assays, enzyme activity measurements, protein extraction, purification, and quantification methods.
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These products range from medical imaging, wearable sensing, in vitro diagnostics, and other high value applications. Knowledge in assembly processes circuit board fabrication, surface mount assembly on circuit boards and higher-level mechanical assembly.
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10+ years of immunoassay development experience in an industrial setting (e.g., in vitro diagnostic, clinical trials, contract research, or pharmaceutical/biotechnology). Deep subject matter expertise in multiple key technical aspects of commercial immunoassay development; including but not limited to protein chemistry, antibody screening, antibody: bead conjugation, assay diluent formulation; multiplexing; preanalytical sample processing; scale-up, assay optimization and troubleshooting; multivariate data analysis; analytical validation; clinical validation.
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The Expression group is responsible for non-GMP protein drug lead generation, supporting the various Pfizer research units and their pre-clinical therapeutic in-vitro and in-vivo needs. The Expression group is responsible for non-GMP protein drug lead generation, supporting the various Pfizer research units and their pre-clinical therapeutic in-vitro and in-vivo needs.
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The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Perform routine testing of pharmaceutical samples by following analytical compendial methods (pH, osmolality, concentration, break-loose extrusion force, etc.
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Maintain, calibrate, and operate instrumentation in the QC laboratory. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
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