Executive Director, Quality Data Analytics & Process - Thousand Oaks

Job DescriptionATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.Executive Director, R&D Quality Data Analytics and Process ManagementWhat you will doLet’s do this. Let’s change the world. In this vital role as the Executive Director, R&D Quality Data Analytics & Process Management, you will lead the strategy, governance, and continuous improvement of core quality processes, document management, enterprise data analytics, and risk management for the Research & Development (R&D) Quality organization.This leader will serve as the business process owner for key Quality Management System (QMS) processes supporting global R&D operations and ensure processes are efficient, compliant, scalable, and aligned with evolving regulatory expectations.A critical component of the role is advancing clinical and research quality analytics across the development portfolio to enable proactive oversight of clinical trials, investigator sites, vendors, and study execution risks. This leader will transform data into actionable insights that strengthen Good Clinical Practice (GCP) compliance, inspection readiness, patient safety, and study quality.The role is accountable for oversight of document management systems and governance, quality process harmonization, advanced analytics, KPI reporting, and R&D risk management across the R&D GxP areas including clinical development, pharmacovigilance, laboratories, and R&D quality systems.This position partners closely with R&D Quality leadership, Global Quality, Global Development Operations, Data Management, Biostatistics, Safety, Regulatory Affairs, and technology functions to strengthen compliance, decision-making, and operational performance. This role will report into Vice President, Quality.ResponsibilitiesStrategic LeadershipDevelop and execute a multi-year strategy for process management, data analytics, document management, and risk management aligned to R&D Quality priorities.Serve as a strategic advisor to the Head of R&D Quality on process performance, clinical quality trends, operational risk, and digital opportunities.Build a high-performing organization focused on innovation, simplification, and measurable business impact.Document and Process ManagementAct as business process owner for core R&D Quality processes such as deviations/nonconformances, CAPA, change control, training(metrics) and risk managementSupport the R&D business process owners to develop global standards, process controls, KPIs, roles/responsibilities, and governance for assigned processes.Ensure simplification, standardization, and modernization of document structures and approval workflows in partnership with Global Quality.Ensure processes are compliant with applicable GxP regulations and integrated across functional boundaries.Lead periodic process reviews, health checks, and continuous improvement initiatives related to these processes.Quality Data Analytics & Data Driven InsightsEstablish a modern analytics strategy for R&D Quality using dashboards, predictive indicators, trend analysis, and self-service reporting tools.Develop executive dashboards for quality performance, compliance health, process efficiency, inspection readiness, and risk visibility.Champion use of automation, AI-enabled analytics, and digital tools to improve decision-making.Develop and lead a comprehensive clinical quality analytics framework supporting risk-based quality management and centralized monitoring across the clinical trial portfolio.Identify cross-study and portfolio-level trends that may indicate systemic GCP risks or process weaknesses in partnership with Clinical & Research Quality.Integrate risk signals from audits, inspections, deviations, vendors, metrics, and operational changes to delivery comprehensive insights.Partner with Clinical Delivery and Study Quality teams to integrate quality signals into ongoing study oversight and risk review forums.Use predictive analytics to identify trials, countries, vendors, or sites at increased risk for quality or inspection issues.Support inspection readiness through analytics related to TMF completeness, overdue actions, protocol compliance, training status, and vendor oversight performance.Develop executive reporting on clinical quality health across Phase I-IV programs, CRO partnerships, and development regions.Benchmark internal metrics against industry trends and regulatory expectations where available.Talent & Organizational CapabilityBuild and develop teams across process excellence, analytics, document management, and risk management disciplines.Develop organizational capability in process thinking, data literacy, and risk-based decision making.Foster a culture of accountability, innovation, and continuous learning.Auto req ID472920BRMinimum Education RequiredHigh School/GEDJob_CategoryEngineeringAdditional Qualifications/ResponsibilitiesWhat we expect of youWe are all different, yet we all use our unique contributions to serve patients. The executive candidate we seek is an experienced leader with the following qualifications.Basic QualificationsDoctorate degree and 6 years of pharmaceutical/biotech quality systems, clinical quality, R&D operations, analytics, or process management ORMaster’s degree and 10 years of pharmaceutical/biotech quality systems, clinical quality, R&D operations, analytics, or process management ORBachelor’s degree and 12 pharmaceutical/biotech quality systems, clinical quality, R&D operations, analytics, or process management AND6 years of managerial experience directly leading people in a multi-tiered organization and/or leadership experience leading teams, projects, programs or directing the allocation of resourcesPreferred QualificationsStrong knowledge of GCP, GxP regulations, ICH E6, risk-based quality management, and quality management systemsDemonstrated success leading analytics, digital transformation, or complex process improvement programsUnderstanding of the legal and regulatory environment, applicable laws, regulations, guidance’s and health authority expectations globally for drug development and digital processes and Artificial Intelligence.Proven track record in management and subsequent response to health authority inspectionsThey will also embody the Amgen leadership attributes which are:Inspire: Create a connected, inclusive, and inspiring work environment that empowers talent to thriveAccelerate: Enable speed that matches the urgency of patient needs by encouraging progress over perfectionIntegrate: Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholdersAdapt: Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver resultsWhat you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $241,844 - $327,200. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.City*Thousand OaksState*CaliforniaJob CodePharmaceutical PharmaceuticalAffiliate SponsorAmgenSalary Range$75,000-$100,000