Senior Manager, Quality Control Analytical

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Company Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease. Why ImmunityBio? - ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases. - Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California. - Work with a collaborative team with the ability to work across different areas of the company. - Ability to join a growing company with professional development opportunities. Position Summary The Senior Manager, Quality Control Analytical will be assigned responsibilities for the management of laboratory testing activities for various programs (fusion proteins, cell therapies and cancer vaccines), routine preventive maintenance, and completing lab administrative duties. The position will be responsible for providing testing support through In Process testing, suitability for use testing, method development, optimizations, transfer, qualification and investigational studies. The analytical testing includes wet chemistry, chromatography (HPLC, Capillary Electrophoresis), spectroscopy (UV-Vis), and ELISA, but not limited to. The position will be required to oversee and coordinate method troubleshooting and investigations. Creating protocols and reports will also be required, using knowledge of GMP/cGMP practices to incorporate the appropriate regulatory requirements into the methods and procedures. The position provides onsite oversight of a wide variety of complex tasks that support the establishment, transfer of the methods into the other QCA lab, and perform various investigational testings. Essential Functions Oversight and scheduling of analytical testing for In Process testing, suitability for use testing, method development, qualification, optimizations, transfer and investigational studies. Oversight of the QC Analytical lab staff, including hiring, training functions, 1:1 meetings, and career development for QCA staff. Interface as QCA member to interact with other departments to coordinate activities. Review of assay protocols and reports in line with commercial GMP standards. Backup analyst for completing assays. Participate and coordinate method development, optimization, transfer, and qualification work (protocol drafting, data collection, and report writing). SOP and Test Method drafting and revisions. Ensure quality control staff, equipment, and procedures are compliant to regulatory guidelines and data integrity principles are adhered to. Performs other projects and duties as assigned. Education & Experience Bachelor's degree in Cell Biology or Immunology or related discipline with 8+ years' of relevant experience in the biotechnology industry with emphasis in analytical development or quality control testing required; OR Master's degree in Biology or related discipline with 6+ years of relevant experience in the biotechnology industry with emphasis in analytical development or quality control testing required Experience with QC testing requirements, methodology and equipment such as HPLC and Plate Readers required Experience leading a team in a GMP environment strongly preferred Demonstrated self and team adaptability under changing circumstances to deliver results Knowledge, Skills, & Abilities Demonstrated understanding of QC testing requirements, methodology and equipment such as HPLC and Plate Readers. Knowledge of cGMP, FDA, and USP regulations and a basic understanding of statistics Knowledge of MS Word, PowerPoint, and Excel Ability to work independently and within cross-functional teams to deliver on project timelines and department goals. Working Environment / Physical Environment This position works on-site in Dunkirk, NY This position works in a lab environment Flexibility in working schedule, i.e., off-hours Must be able to gown and gain entry to labs Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer. Lift and carry materials weighing up to 20 pounds This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. Th