QA Specialist III

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfill their aspirations. Join Kite and help create more tomorrows. Job Description Knowledge: • Demonstrates proficiency in Good Manufacturing Practices (GMPs) and/or Good Laboratory Practices (GLPs). • Demonstrates proficiency in application of QA principles, concepts, industry practices, and standards. • Demonstrates thorough knowledge of FDA / EMEA standards and quality systems, and the interface with other functions like manufacturing, distribution and maintenance. • Demonstrates strong knowledge of six sigma, LEAN and root cause analysis tools used for identifying and correcting deviations • Demonstrates audit and investigation skills, and report writing skills. • Demonstrates strong verbal, technical writing and interpersonal skills. • Demonstrates proficiency in Microsoft Office applications Basic Requirements : • Master’s Degree with 3+ years of relevant GMP or regulated industry experience, including auditing experience; or • Bachelor’s Degree with 5+ years of relevant GMP or regulated industry experience, including auditing experience; or • High School Diploma with 8+ years of relevant GMP or regulated industry experience, including auditing experience. Preferred Qualifications : • Provide QA oversight and approval of deviation, OOS, and change control records that have moderate to significant levels of complexity and /or novelty. • Ensure records are properly initiated, investigated and resolved in accordance with established timelines. •  To provide QA oversight and approval of CAPA and EV records that havemoderate to significant levels of complexity and /or novelty. • Ensure CAPAs are initiated and resolved in a timely manner.• Ensure escalation of deviations per procedures • Identify efficiencies in the execution of the Deviation ad CAPA processes at TCF03 in a compliant manner •  Provide QA support resolving in-process product, final product, manufacturing, environmental, facility and equipment and material issues. • Additional duties as assigned. • These duties can be delegated to designated deputies of a satisfactory qualification level as needed   The salary range for this position is: $107,185.00 - $138,710.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-