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Comprehensive knowledge of GLP regulations, including previous GLP experience in pharmaceutical or biotechnology industry or equivalent GXP transferable experience. Oversee and provide strategic direction for Toxicology/Pathology, BioAnalytical/DMPK, Biomarkers, and Clinical Pharmacology teams to ensure robust support for clinical development programs.
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A minimum of 15 years of related experience including at least five years serving in a Head of IT capacity; biotechnology or pharmaceutical industry experience required. Reporting to the CFO, the VP/Head of IT will oversee delivery of multiple GxP and compliance focused systems and balance the security and strategy of the overall enterprise with the specific needs of Annexon’s business objectives.
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At least 6 years (or 10 years with MSc) relevant direct hands-on experience in drug discovery and development leveraging complex 2D and 3D disease models in biotechnology and pharmaceutical industries.
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A minimum of a bachelor’s degree is required (life sciences disciplines strongly preferred) with approximately 8 years of experience in the biotechnology or pharmaceutical industries in regulatory affairs or related functions in drug/biologics development/manufacturing (an equivalent combination of education and experience may be considered.
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Technical degree in relevant field, such as molecular biology, biotechnology, biochemistry, biology, chemistry, chemical engineering, or biomedical engineering. JD degree from an accredited law school, state bar admission enabling in-house practice (specific state not required), and registration to practice before the USPTO.
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Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.
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5+ years of experience in Pharmaceutical, Biotechnology, or Life Sciences, with a specific focus in Regulatory and working knowledge of Biopharma drug development and approval process. Familiarity with MDM & enterprise reporting capabilities a plus (e.g., Power BI, Qlik, Tableau, or Smartsheet dashboard.
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As the Syneos Health Commercial VP, Business Development you will identify, grow and expand the Syneos Health business development opportunities by developing and leveraging relationships with key decision-makers within biotechnology, pharmaceutical and medical device companies.
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Balazs Nanoanalysis is a contract analytical laboratory owned by Air Liquide Electronics, serving both internal and external clients in industries such as semiconductor, biotechnology, aerospace/defense, solar, energy storage, and automotive.
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Adicet Bio, Inc. is a clinical stage biotechnology company discovering and developing allogeneic gamma delta T cell therapies for cancer. Manage manufacturing activities for viral vector and cell therapy, including cGMP aseptic qualification, in support of manufacturing and formulation of viral vectors as drug substance and of cell therapeutics as drug products.
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Minimum 2 years Manufacturing and product development Pharmaceutical/Biotechnology industry experience (assay validation, product specification setting, OOS, SPC, process optimization, etc. Minimum 2 years Manufacturing and product development Pharmaceutical/Biotechnology industry experience (assay validation, product specification setting, OOS, SPC, process optimization, etc.
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Experience 14+ years clinical trial or drug development experience in biotechnology, pharmaceuticals, or medical device organizations with BA/BS; 10+ years with MA/MS; 7+ years with PhD. The Director in Global Study Operations (GSO) The Director is expected to have a multifaceted role including program, project management, and leading large global teams.
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Minimum of 2 years+ in operations, preferably in the biotechnology or pharmaceutical industry. We are a well-funded startup based in San Francisco in the Dogpatch neighborhood next to UCSF Mission Bay. We have developed a proprietary ultrahigh throughput single cell platform to profile the immune system to find better targets for immunotherapy.
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PhD with 7+ years, Master’s degree with 12+ years, or Bachelor’s degree with 14+ years of experience in a scientific discipline related to biotechnology or pharmaceuticals, particularly in Analytical Development or Quality Control.
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Candidates should be registered to practice before the U.S. Patent and Trademark Office with a strong background in scientific fields relevant to biotechnology. Advanced degree in Biology, Molecular Biology, Cell Biology, Biochemistry or Immunology is desired.
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biotechnology job in South San Francisco, CA
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