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The Quality Control -   Analytics  department  supports  a growing portfolio of  cell and gene therapy  (CGT)   products , including CAR-T, iPSC, AAV, LVV and synthetic DNA products. We  are  immediately  recruiting for a  highly motivated  QC Analyst  I  to perform laboratory testing  with distinct technical but complementary focus  with in a fast-paced GMP environment .  You will  contribute to the development, qualification and execution of analytical methods supporting GMP release and characterization testing.  Additionally, y ou will work cross-functionally with Analytical  / Process  Development , Manufacturing, and Quality Assurance  to ensure methods meet regulatory and compendial expectations while supporting patient safety.  This is an outstanding opportunity for a candidate to  work under the guidance of a supervisor  and mentor , manage time effectively, complete assigned analytical  tasks   in a cross-functional collaborative environment supporting development and cGMP manufacturing of cell and gene therapies.    This role focuses on the development and optimization of  UHPLC-based  biophysical  analytical methods and/or PCR-based, and related mo lecular methods  supporting CGT  safety, identity,  purity ,  strength  and  quality  testing , including   residual impurity and  compendial  applications such as Mycoplasma detection .