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Experience in oncology drug development. Extensive training and experience in the design and conduct of in vitro and in vivo preclinical pharmacology and toxicology studies directed at the development of pharmaceuticals or biologics.
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In addition, the Manager Drug Product Development and Manufacturing will support all aspects of non-GMP and GMP drug product manufacturing and ensure that the CMC team is aligned with the manufacturing strategy at each CMO. A strong knowledge of sterile parenteral filling and the requirements of clinical supply manufacturing is required as well as a working knowledge of cGMP and FDA/EMA guidelines.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Recognized as a subject matter expert around drug product process development and manufacturing for Alexion’s diverse portfolio spanning synthetic, peptide, nucleic acid, AAV and protein-based modalities across various liquid & lyophilized, vial, prefilled syringe, and cartridge-based presentations.
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15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
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Director/Senior Directors of Cell Line Development, Cell Culture Sciences, Purification Sciences, Analytical Sciences, and Drug Product Sciences. The Vice President, BioPharmaceutical Development is a strategic leader responsible for oversight of Cell Line Development, Cell Culture Sciences, Purification Sciences, Analytical Sciences and Drug Product Sciences.
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Data Strategy Development: Define and implement a comprehensive data science strategy aligned with the company's R&D objectives, ensuring data science and AI/ML methodologies accelerate target discovery, drug development, and biomarker identification.
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Evaluate and develop the most appropriate biochemical and biophysical characterization tools to support biological drug product development, including adjuvanted vaccine drug products.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Background in, or deep understanding of modern synthetic organic chemistry, as well as of the drug substance development process, process chemistry, and pharmaceutical manufacturing, and their interrelationship with analytical development is essential.
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As a Drug Alcohol Counselor, you will be responsible for developing, facilitating and evaluating substance abuse treatment services and facilitating the completion of the Pathways curriculum according to the request of the Placing Agency and the needs of the students.
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Previous experience with genetic medicine, viral vectors, gene therapy, AAV, gene editing drug development/toxicology/regulatory interactions or ocular toxicology/drug development/regulatory toxicology experience is strongly preferred.
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As the Senior Managing Counsel, you will play a critical role in advising and guiding our organization on legal matters related to clinical trials, drug development, regulatory compliance, and other legal aspects specific to the oncology field.
$228,400 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Working knowledge of Drug Safety/Pharmacovigilance processes (Intake, Safety Case Processing, Expedited Reporting, Periodic Reports, and Document Management, Report Writing/Analytics) by leveraging any related software.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The VP of Drug Safety and Pharmacovigilance will provide the leadership and management for the infrastructure of the Drug Safety and Pharmacovigilance department across both clinical development and commercial products for the company.
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You have strong expertise in immuno-oncology and will be focused on focus on the development of fit-for-purpose CMC assays using flow cytometry and cell-based immunoassays, to characterize engineered TCR-T cell drug substance and drug product.
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Strong understanding of science and drug development, with specific expertise in nonclinical study design, preclinical CROs, data management systems, nonclinical study procedures, and statistical analysis methods.
$300,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
drug development jobs Title: senior accountant Company: Charles River Laboratories
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