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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 .
Salary estimate
$41,000 – $55,000/yr
Provided by the employer.
Skills for this role
Recruiting
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Interview preparation
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