Dragonfly Therapeutics
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As an IT Infrastructure Lead, you will own the technical management of IT systems and infrastructure, ensuring reliability and security. Responsibilities include planning and managing networks, configuring servers, maintaining laboratory IT systems, leading change management, and collaborating with teams to address IT challenges and enhance user experience. Additionally, you will work on data protection, cybersecurity, and vendor management.
The Associate Director of Downstream Process Development will lead and optimize downstream processes for the purification of bispecific antibodies and other biologics, ensuring compliance with regulatory standards. Responsibilities include mentoring junior scientists, overseeing process scale-up and technology transfer, and collaborating with cross-functional teams to deliver on production needs.
The downstream process development engineer will collaborate with R&D and Tech Ops teams to develop and optimize processes for biologics, enhance production methods, and troubleshoot technical challenges. Responsibilities include developing scalable production processes, running analytics, and preparing documentation.
The Head of Quality will lead the Clinical Quality Assurance function, developing and implementing QA strategies to ensure compliance with regulatory requirements. Responsibilities include managing GXP oversight, engaging with executive management, leading vendor quality oversight, and delivering training programs for quality improvement.
The Principal Associate Scientist/Scientist I will perform biophysical and biochemical characterization of candidates including comprehensive protein analytics. Responsibilities encompass developability assessments, data interpretation, technical reporting, assay development, and maintaining high documentation standards. Collaboration with cross-functional teams is essential while managing laboratory operations and equipment maintenance.
The Senior Scientist in CMC Analytics will leverage expertise in biochemical and biophysical assays to support drug discovery and immunotherapy programs. Responsibilities include method development, data interpretation, process support, and regulatory submission documentation, while collaborating with cross-functional teams to advance clinical candidates.
The Associate Scientist II/Sr. Associate Scientist will conduct biophysical and biochemical characterization of therapeutic candidates, perform developability assessments, analyze data, author technical reports, and collaborate with cross-functional teams to drive candidate selection and project goals.
The Director of Analytical Development will lead the development, optimization, and tech transfer of analytical assays for the testing of clinical-stage biologics. Responsibilities include mentoring teams, ensuring regulatory compliance, and collaborating with multiple departments to advance product development.