Quality Control Analyst - GMP

Compensation:$33.75hr to $39.50hr.Exact compensation may vary based on several factors, including skills, experience, and education.Healthcare benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, financial protection benefits, as well as HSA, FSA, and DCFSA account options. 401k retirement account access is offered starting on the 90th day with employer matching after one year of service. Employees in this role are also entitled to paid sick leave andor other paid time off as provided by applicable law.Required Skills & Experience-Minimum one year of relevant GMP work experience in a lab setting -Bachelor degree in Biology or Chemistry -Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs) -Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, andor ELISA -Ability to readinterpret technical documents such as SOPs, work instructions, test methods and protocols -Proficient with Microsoft Office applicationsNice to Have Skills & Experience-1 year of experience working with mammalian cell culture-CAR-T, Cell and Gene Therapy, or Biochemistry laboratory experience-Basic knowledge of Compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC-Ability to complete equipment and software qualification protocols -Experience developing and setting long-term objectives-Experience working in Biosafety Level lab (BSL 2, BSL2+) or aseptic facility-Knowledge of EUFDA guidanceJob DescriptionThe QC CRS Analyst is responsible for conducting biochemical and testing of raw material, in-process, final product release and characterization samples, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 -- 10 other Analysts within a functional Clinical Release and Stability Laboratory and report to the Senior QC Supervisor.Key Responsibilities:-Conduct analytical biological testing of clinical and commercial drug productdrug substance samples-Perform peer reviews and approvals of laboratory data-Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing including application of statistical concepts to laboratory data-Support of New Product Initiatives (NPI) including owning a project and perform project management functions with limited to no coaching from supervisionmanagement-Perform Instrument Calibration and Preventative Maintenance-Update CRS-owned documents using the Document Management System (DMS)-Orderreceive supplies and manage inventory-Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities-Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight-Act as a peer subject matter expert in assessing talent by participating in panel interviews for job-Complete invalid assay and general laboratory investigation records-Complete corrective and preventative actions (CAPA) as assigned-Assist in the execution of internal audits

Created: 2025-02-24