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Executes Design of Experiments (DOE) and Proven Acceptable Range (PAR) experiments to support design space understanding and process validation as they relate to oligonucleotide synthesis, process chromatography, and other purification and isolation techniques.
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Industry giant seeks an experienced Process Development Scientist to develop protein purification processes to be scaled up and transferred into cGMP manufacturing including evaluation of transferred processes, transfer of processes to manufacturing, harvest clarification, normal flow filtration, purification, tangential flow filtration, and product final formulation.
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Join our Process Development Team in using a variety of fermentation techniques, purification techniques, and characterization methods to support commercial and bench scale pharmaceutical processes.
$34 - $34.64 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Research Associate I position will support process development by assisting in the development of methods for generation and purification of various bacteriophages. Experience in upstream and downstream process development scale-up.
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The Director of Purification Development for Pre-pivotal Biologics will be responsible for leading molecular assessment, purification development, process transfer and implementation at manufacturing facilities to produce drug substances for toxicology and pre-pivotal clinical studies.
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Ability to identify, develop and implement solutions to practical problems through application of fundamental scientific and engineering principles, preferably in a process development environment.
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This role is in an integrated bioprocess development group in which cell culture and purification scientists work together to advance rich, exciting and dynamic pipeline. The successful candidate will design and execute experiments at the bench scale, spanning the end-to-end drug substance process, including both cell culture and purification operations.
ExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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As a CMC development lead, the individual will apply their strong expertise in CMC fermentation and/or purification to develop robust, phase-appropriate processes for drug substance GMP production to enable human clinical studies and eventual licensure.
$200,000 - $240,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Process development and product development for new vape, concentrate, and infused products. Conduct extraction process development work from bench top pilot projects through production scale batches, via experimental design and process validation.
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Scientist - Downstream Process Development. We are seeking a highly skilled and motivated Scientist to come join our CMC, Process Development team and help drive our clinical trials to market.
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Support early & late-stage CMC development activities including cell line development (CLD), cell culture development (CCD), & purification development for product quantitation, product quality & process impurities for biologic molecules.
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Biopharmaceutical Development and Manufacturing Services Beyond supplying high quality proprietary APIs, we provide contract process development & cGMP manufacturing services, including heparin derivatives, natural products extraction, fermentation and purification.
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The ideal candidate should have prior process development experience with common purification techniques such as clarification, chromatography, UF/DF and ultracentrifugation. This role is responsible for supporting process development for viral vector purification for internal and client programs.
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Biologics process development experience, particularly designing and scaling up of bioreactor and purification processes for protein therapeutics. Process Engineering, a part of AbbVie R&D’s Development Sciences organization, is responsible for designing and developing scalable processes to make small molecule drug substances and drug products, including antibody drug conjugates (ADCs), throughout pre-clinical and clinical development stages.
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Solid working knowledge of various manufacturing platforms (Microbial fermentation process, IB recovery and refolding, CHO cell culture and purification, Pegylation, PEGylated protein purification etc.
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