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Understanding of standard drug development process, defining in vivo pharmacology, assessing PKPD and deriving margins to provide clinical starting doses. Conceptualize and design strategies for drug discovery using insitro's platforms from hit to lead using industry standard preclinical pharmacology models and standard drug development models by applying insights exposed by insitro's unique target discovery credentialization.
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Forms cross-functional alliances with Small Molecule Drug Substance Development, Small Molecule Drug Product Development, CMC Regulatory Affairs, Quality Control and Manufacturing Operations by providing SMEs to these functions and project teams.
$221,170 - $286,220 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Implement and configure Enovia modules according to business needs, including but not limited to Product Data Management (PDM), Change Management, and Engineering BOM Management.
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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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Responsibilities -Develop assays for GMP release of gene therapy products-Develop assays for product characterization of gene therapy products-Develop assays for AAV/protein/DNA to assist in evaluation of process change, formulation andstability study-Report project status (development plans, timelines, and results) to supervisor and technical teams.
$36.11 - $40.54 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director of CMC Analytical Development's responsibilities will be:Create and put into place CMC analytical strategies to assist with drug development and regulatory submissions.
$200,000 - $245,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Skydio team combines deep expertise in artificial intelligence, best-in-class hardware and software product development, and operational excellence to empower a broader, more diverse audience of drone users - from action sports enthusiasts to first responders to insurance claims adjusters.
InternExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Minimum 3+ years of operating or product experience including leading projects and a track record of exceeding KPIs or 3+ years of management consulting or other team-based client-facing experience.
$150Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strengthen internal gene therapy CMC capability and serve as regulatory subject matter expert and influential leader within the R&D organization to contribute to drug development at Adverum for its development programs.
$250Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Minimum of 5 years of experience in product management within the biotech, pharmaceutical, or life sciences industry, with a focus on synthetic DNA or molecular biology products. We are seeking an entrepreneurial and visionary Senior Product Manager to lead the strategic development and commercialization of our synthetic DNA offerings in the mRNA and genetic medicine markets.
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Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
$140,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Deeply involved in design and development of GWCP/ATMOS - infrastructure as code using technologies such as EKS (Kubernetes), Terraform, Golang. Prior experience with Infrastructure as Code and configuration management, using tools like Terraform and Ansible.
$125,000 - $175,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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What you will do:The Global Development Scientist Director is an important part of the Clinical Project Team (CPT), and Global Study Team (GST) working harmoniously and cross functionally (in a matrix environment) with other CPT & GST members, Site Management & Monitoring (SMM), field-based liaisons, and site personnel.
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Proven experience in the integration and management of PDM, and PLM systems for the product development life cycle within a manufacturing or engineering environment. , ECO process, product structure, configuration engineering, change management, and revision control and tracking.
$150Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Expertise/Advanced knowledge of biotechnology products, market dynamics, and regulatory requirements with strong disease knowledge in rare diseases, neurology, ophthalmology, and/or immunology drug development.
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product development management drug jobs Title: director in San Mateo, CA
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