Research Associate 1
Research Associate 1
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Job Description
Preferred Qualification and; Experience:./MTech Biotechnology with 2 7 years; experience in developing manufacturing and characterizing CAR cell therapy products and understanding of Cell Therapy Research and associated regulatory Skillset & Competencies:CART manufacturing under GMP settingsupstream processingMammalian cell cultureQMSExperience in Biosafety cabinet and aseptic operationsCulture of T cells/NK cells and handling of viral vectorsStatistical analysis Presentation & Communication SkillsDocumentation and Report WritingRoles & Responsibilities:Responsible for optimization of CAR cells manufacturing processes using normal human or patient derived primary blood components following ethical practices and QMS as per GMP guidelinesActively engage in the manufacture of CART cell therapy products by diligently prioritizing the lab functions to meet critical and carefully execute transduction by viral vector and nonviral vectorbased approaches activation and expansion of immune cells (T cells NK cells etc) isolated from clinical specimens without compromising sterility and quality parameters as per the guidelines and defined criteria by maintaining highest to communicate effectively in a highly matrixed team environment to advance the company’s cell therapy pipelineParticipate and assist in technical transfer and core R&D activitiesTo review and document SOPs protocols and reports pertaining to the program closely with crossfunctional teams to design and implement cell therapy processes and workflow for cell therapy platformsProvide critical technical/scientific recommendations for the manufacturing process improvementsWork with vendors to evaluate raw materials and consumables for compatibility with the Manufacturing processCoordinate very closely with quality control quality assurance supply chain teams etc and strictly adhere to the project timelines by preserving integrity accuracy safety and qualityPrepare for and participate in compliance monitoring inspections / regulatory agency to troubleshoot experiments record analyse interpret and present the data in scientific of systems and process pertaining to sterile practices work ethics safety health and environment.
Required Experience:
IC
Employment Type
Full-Time
