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Since Camargo Pharmaceutical Services is the leading expert in drug development, you will provide expertise and customer-centric professionalism to our clients, which range from small biotech firms to large, established pharmaceutical companies.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Marken offers a state-of-the-art GMP-compliant depot network and logistic hubs for clinical drug product storage and distribution worldwide, and supports cell and gene therapy logistics services from clinical to commercial, while maintaining the leading position for Direct-to-Patient and Home Healthcare services, biological sample shipments and biological kit production.
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A deep knowledge of cancer biology and immune-oncology and drug development across different modalities - small molecules, biologics, gene, and cell therapy. Xilis, Inc. has been developing cutting-edge Patient-Derived Micro-OrganoSpheres (MOS) technology for precision cancer diagnostics and drug development in the Research Triangle Park in Durham, NC. Xilis' transformative platform recreates patient-specific tumors in their 3D and environmental complexity at micro-scale ex vivo, allowing high-throughput, clinically relevant, and affordable experimental selection of the most effective drugs for every patient in a matter of days.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Comprehensive knowledge of the clinical and pharmaceutical drug development process. The role involves integrating strategy, design, feasibility and operational planning to produce business-focused clinical drug development programs that align with AstraZeneca priorities and strategy.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Director for Downstream Process Development, you will develop, design and transfer downstream processes for a variety of product candidates spanning early and late stage development and multiple modalities (including complex Fc fusion proteins, mAbs and mRNA) at Shattuck Labs. You will lead the downstream process development team and coordinate efforts with multiple teams across R&D and Technical Operations to deliver downstream processes for our pipeline of drug candidates.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Under the supervision of an R&D Manager, the candidate will help with the development of new chemical formulations and/or biomaterials (hydrogels, coatings, resorbable polymers, viscoelastic materials etc.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience of life-cycle management including clinical line extensions of the drug development process in regulatory affairs preferred. We are looking for an ambitious Manager/Associate Director of Regulatory Affairs to ensure the development of appropriate global and/or regional regulatory life-cycle strategy(s) and their execution for assigned products to meet the needs of the business.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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ResponsibilitiesExecute analytical methods for in-process control, release testing and stability monitoring of bulk drug substances and drug products under cGMP guidelinesParticipates in experimental design, including development of methods and testing requirements to demonstrate method suitability.
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Lead a Quality Assurance organization responsible for raw material inspection and release, QA on the floor, disposition of bulk drug substance, QA review of quality control data, and QA review of method validation, process validation, and equipment/utilities qualification.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Hands-on experience with mobile feature development and testing is a must (XCUI for iOS or Espresso for Android) Where permitted by federal or state law, Fidelity will also conduct a pre-employment drug screen, which will review for the following substances: Amphetamines, THC (marijuana), cocaine, opiates, phencyclidine.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Expert in computer technology quality and compliance (including computerized system validation) and the pharmaceutical industry across multiple disciplines within Clinical Drug Development (Phase I/II/III/IV) and/or Manufacturing.
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Granite Construction is an Affirmative Action/Equal Opportunity Employer of Minorities, Females, Protected Veterans, Individuals with Disabilities and a Drug-Free Workplace. This position is accountable for administering regional recruiting, employee relations, benefits, compensation, training and development, talent management and labor relations to ensure alignment with the company’s Human Resources objectives and maximize employee engagement.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The Sr. Product Development Scientist/Associate Director will Assist with the coordination, management, and execution of Phase I through Phase IV clinical studies and support the conduct of preclinical studies to ensure the successful submission and approval of a drug product by regulatory agencies.
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Knowledge of Life Science or Pharma Market and drug development life cycle - preferred. Identifies and qualifies leads and support/lead in Business Development and Sales activities, thereby contributing to new business wins.
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Experience with agile development methodologies and agile planning tools such as Jira and Azure DevOps. Experience with agile development methodologies and agile planning tools such as Jira and Azure DevOps.
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drug development jobs in Durham, NC
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