Supervisor, Quality Control

Job Description Shift: Wednesday–Saturday, 12:00pm–10:30pm Specific Responsibilities Lead a team of high‑performing individuals, with particular focus on individual development in support of greater team achievement. Drive a culture of Operational Excellence in the group. Supervise Analytical QC testing and various other support activities performed in the Analytical QC Lab. Review records, generate CoAs for product release, and complete routine record review of test data and related documents for in‑process testing, drug substance, and drug product release. Oversee on‑time completion of training for the group. Monitor GMP systems to ensure compliance with documented policies. Adopt a hands‑on, collaborative approach to problem solving, planning, and people‑management. Support development and implementation of Operational Excellence initiatives to enhance laboratory and staff efficiencies. Participate in and/or lead daily and weekly team meetings. Work with internal and external resources to maintain analytical equipment in an optimal state. Oversee purchase and qualification of equipment, materials, and media required for routine testing and reagent qualification. Manage OOS, lab and protocol deviations, and implement corrective action plans when necessary. Provide input and support in the development, revision, and review of SOPs, protocols, and reports. Participate in inspections by both internal and external stakeholders as needed. Basic Qualifications MA / MS Degree with 3+ years of analytical and/or cGMP operations and/or quality experience OR BA/BS Degree with 5+ years of analytical and/or cGMP operations and/or quality experience OR High School Degree with 9+ years of analytical and/or cGMP operations and/or quality experience Preferred Qualifications Experience supervising/managing analytical labs within the biotechnology or pharmaceutical industry. Demonstrated guidance and overseeing skills, including establishing direction and goals, and guiding implementation while fostering a team‑based environment. Excellent interpersonal, verbal, and written communication skills. Experience with Flow Cytometry, PCR, ELISA, or cell viability measurement. Familiarity with FDA, EU, and ICH guidelines. Working knowledge of quality systems and regulatory requirements (21 CFR Part 11/210/211), Quality Control, GMPs, GLP. Comfortable in a fast‑pace company environment with minimal direction and ability to adjust workload based on changing priorities. Ability to think critically and demonstrate troubleshooting/problem‑solving skills. Excellent skills in Microsoft Office, data analysis software, and related applications. Salary Range: $107,185.00 – $138,710.00. The position may also be eligible for discretionary annual bonus, discretionary stock‑based long‑term incentives (eligibility may vary), paid time off, and a benefits package. Benefits include company‑sponsored medical, dental, vision, and life insurance plans. Kite Pharma is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long‑term durable response and eliminating the burden of chronic care. Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non‑job related characteristics or other prohibited grounds specified in applicable federal, state, and local laws.

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