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The Chemist will: Plan and safely conduct laboratory experimentation Set up equipment, prepare, characterize and test formulation properties, Utilize a range of analytical and applications testing equipment to collect data and solve problems.
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PhD with 15 yrs or MS with 20 yrs experience in scientific leadership positions, including significant work experience in protein biochemical analysis, cGMP Quality Control, and analytical development in an FDregulated industry.
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This role will focus on developing analytical methods supporting biologics, cell, and gene therapy modalities. The ideal candidate will possess a deep understanding of tissue culture, cell line maintenance, cell-based assays, and proficiency in molecular approaches such as DNA/RNA extraction and PCR techniques.
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Perform routine cGMP testing of samples for biopharmaceutical clients in a BSL-2 laboratory which may include HPLC, SEC, CE-SDS, cIEF, MDI/MFI, GC, UV-VIS spectroscopy (A280 and SoloVPE), oligosacharride mapping, turbidity, and/or osmolality
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At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission.
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Title: Associate Scientist/Scientist, BCGT Analytical Development. Associate Scientist/Scientist, BCGT Analytical Development. Reports to: Director, BCGT Analytical Development. Title: Associate Scientist/Scientist, BCGT Analytical Development.
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We are partnered with an innovative biotech company who is seeking an experienced analytical scientist to join their Quality Control group in overseeing and conducting testing, ensuring high quality products.
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Title: Quality Control Analytical Scientist. Familiarity with analytical equipment including UV absorbance plate readers, Flow cytometers, microscopes, automated cell counters, and PCR thermal cyclers.
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A dynamic medicinal chemist, that drives medicinal chemistry functions for drug discovery projects, working in concert with molecular and cellular biology, pharmacology, ADME, structural biology, and other key functions.
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Provide scientific, regulatory, and compliance oversight to the Biologics Analytical Technologies group responsible for analytical methods developed, optimized and performed to support preclinical, phase I through phase III clinical trials including raw material testing; in process, characterization and release bulk drug substance testing; and stability study testing for BDS and DP. Also, supports Phase III/licensure by technology transfer to external partners.
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2-4 yrs working experience in a cGMP Quality Control, analytical development, analytical transfer or validation department in a FDregulated industry. HPLC, capillary electrophoresis, ELISA, or SDS-PAGE, used for analysis of recombinant proteins.
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Title: Manufacturing Technician (Analytical Instrument Manufacturing Experience required - 6 months min) at Mainline Scientific, LLC. This role would report into the design and manufacturing arm of analytical instruments.
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