Adverum Biotechnologies
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The QA Director of GxP Compliance leads corporate-wide GxP initiatives to ensure adherence to regulatory requirements and quality objectives. Responsibilities include strategic leadership, developing quality processes, overseeing compliance programs, and collaborating with cross-functional teams.
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The Director of Process Development will lead the Downstream PD team to develop compliant and high-quality AAV production platforms. Responsibilities include process characterization/validation, process performance qualification, technical management at CDMOs, and collaboration with various functions within the company.
The Associate Scientist will be responsible for developing and validating optogenetic gene therapy vectors, executing assays for discovery and translational research, and supporting preclinical and clinical assays. They must have a minimum of 6-8 years of relevant experience in molecular biology and microbiology techniques.