Senior Regulatory Labeling Associate

Kite Pharma • Santa Monica, CA

4d

About The Position

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 fulfil their aspirations. Join Kite and help create more tomorrows. Job Description The Senior Associate, Regulatory Labeling supports and executes the preparation, maintenance, and implementation of regulatory labeling content for assigned investigational and/or marketed products. This role contributes to global and regional labeling activities across the product lifecycle and serves as a knowledgeable operational resource to cross functional partners. The Senior Associate is expected to work effectively in a fast paced, matrixed environment, demonstrating flexibility in managing shifting priorities and timelines while maintaining a high level of accuracy, compliance, and inspection readiness. The role supports continuous improvement initiatives and the evolving use of digital tools, systems, and emerging technologies—including automation and AI enabled solutions—to enhance labeling execution and compliance.

Requirements

• 5+ years of relevant industry experience and a BA or BS Degree in a scientific field is preferred.
• Experience supporting labeling activities for investigational and/or marketed products.
• Familiarity with U.S. and international labeling regulations and health authority expectations.
• Experience working in cross‑functional, matrixed environments.

Responsibilities

• Will supports and executes the preparation, maintenance, and implementation of regulatory labeling content for assigned investigational and/or marketed products.
• This role contributes to global and regional labeling activities across the product lifecycle and serves as a knowledgeable operational resource to cross‑functional partners.
• Expected to work effectively in a fast‑paced, matrixed environment, demonstrating flexibility in managing shifting priorities and timelines while maintaining a high level of accuracy, compliance, and inspection readiness.
• The role supports continuous improvement initiatives and the evolving use of digital tools, systems, and emerging technologies, including automation and AI‑enabled solutions to enhance labeling execution and compliance and global Regulatory submissions is required.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees