Associate Director, Global Quality Systems - Document Control and Training

* Provide strategic direction and oversight for the Global Document Control program.* Establish and monitor key performance indicators (KPIs) to assess program effectiveness.* Conduct regular audits and assessments to ensure compliance with document control requirements.* Identify and mitigate risks associated with document management.* Ensure alignment with applicable regulations (e.g., FDA, ISO), internal policies, and business needs.* Manage interdependencies within and across QMS Topics.* Provide leadership and technical direction for their Topic and associated support systems across a Global network.* PhD with 2+ years of related experience in a biologics or pharma organization OR* MS/MA with 8+ years of related experience in a biologics or pharma organization OR* BS/BA with 10+ years of related experience in a biologics or pharma organization* High School diploma with 14+ years of related experience in a biologics or pharma organization* 10+ years of experience in the pharmaceutical and/or biotechnology industry operating within, or managing, a global document control network.* Experience with Veeva eDMS is preferred* Excellent communication and influencing skills* Proven ability to work and influence across a global network* Ability to collaborate and work cross-functionally* Creative problem solving approach and solutions based mindset* Ability to provide cross-functional leadershipEveryone at Kite is grounded by one common goal – curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work. #J-18808-Ljbffr