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Supports lifecycle management of products from ideation, development, and commercialization for all Tandem products across different product portfolios; drives for innovation in all aspects of product development.
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Director of Drug Product Development and Manufacturing based at our San Diego office. In this role, you will be responsible for leading projects focused on formulation design and optimization, formulation process development and characterization of the most exciting CAR- tLNP drug product, to support emerging research pipelines focused on autoimmune, oncology, fibrosis and inflammation-related diseases, as well as blood monogenic disorders.
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Strong scientific and business acumen - the ideal candidate will have in-depth medical, scientific, regulatory, and technical knowledge of most functional areas involved in drug discovery, platform and/or clinical drug development.
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Cellics Therapeutics is seeking a Principal Scientist/Associate Director, Upstream Process Development and Manufacturing to lead the execution of CMC strategies in cell culture process development and manufacturing in support of our drug development and regulatory filings.
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Perform additional duties as assigned by the Director of Land Development. Regular review of project development budgets with Director of Development for reconciliation.
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We are working with an Artificial Intelligence-driven Drug Discovery (AIDD) team in San Diego on a Director of Biomarker Implementation/Clinical Data management. 💻 Director of Biomarker Implementation/ Clinical Data management- Oncology.
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Education and Experience:Bachelors in a scientific discipline and 10+ years of work experience and 3+ years of management experienceExperience in leading and developing high performance teamsBackground in a relevant scientific area, such as drug discovery, therapeutic development, computational chemistry, computer vision, statistics, artificial intelligence, modeling, simulations computational genomics or biology, statistical genetics, data science, chemistry, or biology.
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The Senior Manager of Drug Safety & Pharmacovigilance (PV) Quality, is a key role and is responsible for oversight of Drug Safety & PV quality, compliance, and alliance management activities, thus always promoting inspection readiness and maintaining a robust global compliance program within the Quality Assurance department.
$150,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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You'll be responsible for designing, executing, and reporting on the analytical development of small molecule chemistry experiments, degradation pathways, characterization, and stabilization techniques for ophthalmic and injectable drug products.
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Business Development Manager. Project management and multitasking capability. From water and flood damage, to fire damage and mold remediation, Paul Davis franchise professionals are available 24/7 to clean up and repair damage to residential and commercial property.
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Strong track record in drug product development, CDMO management, and large-scale manufacturing. The Senior Director overseeing Drug Product Development will lead the integration and supervision of all aspects of product development, encompassing pre-formulation sciences, formulation development, device development, and packaging development.
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Engage in business development activities to source and close SBA loan requests. The SBA Business Development Officer position is responsible for soliciting, negotiating and developing new business for the bank’s SBA department as well as the bank’s other products in compliance with the Bank’s policies and procedures.
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The Development Director is part of the Executive Management Team and is responsible for planning, developing, leading and maintaining a comprehensive and successful fundraising program on behalf of the Legal Aid Society of San Diego (LASSD.
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Create global value dossiers, cost-effectiveness and budget impact models and market entry plans for in-country Health Technology Assessment (HTA) and pricing & reimbursement submissions, within product development timelines.
$291,000 - $321,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are committed to leadership in advancing the science and technology of molecular glue drug discovery, while prosecuting a pipeline of projects through clinical development. Assay development, optimization, and data collection for the purposes of fragment identification and validation, SAR studies, and mechanism of action studies using various assay formats.
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product development management drug jobs Title: development director Company: Omeros in San Diego, CA
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