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Support drug candidate design optimization, selection, validation, and stability study throughout pre-clinical and clinical purification process development for antibody/protein. Support and closely work with research, cell-line development, upstream, downstream, and analytical scientist.
$90,000 - $120,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience in biopharmaceutics/drug absorption, related tools (in-vivo, in-vitro, in-silico), and product design and development. Familiarity with regulatory biopharmaceutics requirements and drug development processes.
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Ensures the effectiveness of the CMC Regulatory team in developing submissions and in working across functions (such as Drug Product Development, Drug Substance Development, Analytical/QC, and Quality teams.
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This position will also collaborate with other scientists, including bioinformatics, in vivo pharmacologists, and other external scientists across academia and industry to advance the pipeline from idea to clinical development.
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Ensures all development and technology transfer activities are aligned with Nephron Pharmaceuticals Corporation's project goals and timelines. Nephron Pharmaceuticals Corporation is a privately owned global leader in the manufacturing of generic drug products, over-the-counter (OTC) drug products and medical devices.
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Ensure development of phase-appropriate drug substance processes for portfolio of bispecific antibodies and cytokine fusion molecules, including cell banking, upstream cell culture, and downstream purification.
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The Staff Scientist - Drug Product Development will assume the critical role of overseeing and executing investigations while developing and deploying strategies aimed at resolving a range of product-related challenges, extending from the initial stages to the more advanced phases of drug product development.
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In-depth understanding of the drug development process, from nonclinical development to product registration, post-approval requirements or commitments and life-cycle management with a working knowledge of non-clinical development, early- and late-stage clinical development, clinical operations, regulatory affairs, drug safety and pharmacovigilance, drug manufacturing and supply, market access, and commercial functions.
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Represent Lab QA in risk assessment activities for Drug Substance, Drug Product, and Analytical Development. Specifically, this position will provide quality oversight on our state-of-the-art analytical capabilities, clinical assay development and validation, biomarker assay validation and clinical product testing to support both viral vector manufacturing and clinical development.
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1 to 5 years of ETL development experience with any leading platforms (Informatica/SnapLogic/Dell Boomi/Talend/Sterling Integrator) Dell Boomi development experience. We maintain a drug-free workplace and perform pre-employment substance abuse testing.
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Serve as clinical pharmacology lead and pharmacometrics representative on multiple project teams and support model-based drug development strategies for ongoing projects. Great working knowledge of formulation development, drug development and clinical development.
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The Peer Recovery Specialist provides non-clinical services and support the screening and follow up process intended to aid patients in establishing recovery from high risk of dependent alcohol and drug use problems.
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Freeport-McMoRan promotes a drug/alcohol-free work environment using mandatory pre-employment drug testing and on-going drug and alcohol testing, as allowed by applicable laws. Freeport-McMoRan promotes a drug/alcohol-free work environment through the use of mandatory pre-employment drug testing and on-going random drug testing as allowed by applicable state lawsWhat We Offer You The estimated pay range for this role is currently $23.00.
$23 - $30 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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HPOne requires the necessary drug testing and background checks as part of our pre-employment practices. The Leadership Development Program participant will be provided with in-depth experiences, ongoing mentorship, and targeted training across a range of business areas within HPO spanning an 18-month period.
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Amgen is seeking a Process Development Senior Associate to join the Pivotal Drug Substance Technologies (DST) organization in Cambridge, MA. The pivotal DST organization is responsible for developing cell culture and purification manufacturing processes for Amgen’s late-stage pipeline.
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