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Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Associate Director - Operational and Digital Enablement, Regulatory Affairs CMC

Business OperationsConfirmed live in the last 24 hours
Full-timeFoster City, CA, USAHybrid

About the Job

Requirements

  • At least 10 years of experience with a Bachelor of Science or Bachelor of Arts degree, or at least 8 years of experience with a Master of Science, Master of Arts, or Master of Business Administration degree.
  • Experience in regulatory operations, CMC Regulatory Affairs, pharmaceutical development, or a related regulated environment.
  • Demonstrated experience leading business process design, mapping, optimization, or operational improvement initiatives.
  • Experience translating business needs into requirements and partnering with technology teams to implement digital or system-enabled solutions.
  • Experience leading complex, cross-functional initiatives in a global and highly matrixed organization.
  • Strong understanding of pharmaceutical regulatory processes and the regulatory lifecycle; experience with CMC regulatory processes is strongly preferred.
  • Familiarity with regulatory information management, document and content management, workflow, data, analytics, automation, or artificial intelligence-enabled solutions.
  • Ability to analyze complex problems, structure ambiguous issues, develop recommendations, and drive work through implementation.
  • Ability to facilitate effectively, gather subject matter expert input, and translate it into clear, practical end-to-end processes and requirements.
  • Ability to communicate and influence effectively across functions and organizational levels.

Responsibilities

  • Lead business process mapping, analysis, design, and optimization initiatives across CMC Regulatory Affairs, including development, registration, post-approval, and lifecycle management activities.
  • Identify operational pain points, process gaps, inefficiencies, and opportunities for simplification or digital enablement with process owners and subject matter experts.
  • Apply structured problem-solving and data-driven approaches to evaluate root causes, assess options, and develop practical, sustainable solutions.
  • Facilitate cross-functional workshops and working sessions to define current- and future-state processes, clarify roles and decision points, and establish implementation plans.
  • Support development and maintenance of process standards, procedures, governance mechanisms, and operational controls that enable consistent execution across CMC Regulatory Affairs.
  • Develop and monitor operational measures and key performance indicators to evaluate process performance, adoption, and continuous-improvement opportunities.
  • Support portfolio, resource, and operational planning activities, including use of enterprise planning and resource forecasting tools.
  • Partner with the CMC Digital Enablement Head, business process owners, information technology, and other stakeholders to identify and advance digital opportunities addressing regulatory business needs.
  • Translate regulatory operational needs and process requirements into clear business requirements and use cases for digital, automation, data, and technology solutions.
  • Lead or support implementation of digital solutions from business problem definition and requirements development through testing, deployment, adoption, and continuous improvement.
  • Establish and monitor success metrics for digital and artificial intelligence-enabled capabilities, including adoption, operational efficiency, quality, user experience, and business value realization.
  • Evaluate opportunities to apply workflow automation, analytics, artificial intelligence, and emerging technologies to improve regulatory processes and decision-making.
  • Support integration of regulatory processes, data, content, and systems to enable more connected and efficient ways of working.
  • Partner with data and system owners to improve data quality, usability, and availability for regulatory operations, analytics, and decision-making.
  • Develop dashboards, metrics, and operational insights that increase performance visibility and enable data-driven decisions.
  • Support user acceptance testing, implementation readiness, change management, and adoption of new or enhanced digital capabilities.
  • Lead complex cross-functional initiatives involving CMC Regulatory Affairs, Regulatory Affairs, Technical Development, Quality, Manufacturing, Supply Chain, Strategy and Operations, information technology, and other relevant stakeholders.
  • Establish clear project objectives, scope, deliverables, roles, dependencies, and implementation plans for assigned initiatives.
  • Build alignment among stakeholders with differing priorities and translate complex operational or technical topics into clear business decisions and actions.
  • Develop recommendations and decision materials for CMC Regulatory Affairs leadership based on analysis of operational challenges, opportunities, risks, and potential solutions.
  • Partner with Regulatory Policy, Intelligence, and Health Authority Strategy colleagues to ensure processes and solutions remain aligned with evolving global regulatory requirements and expectations.
  • Drive organizational change initiatives to implement new processes, digital tools, and artificial intelligence-enabled ways of working, including stakeholder engagement, communications, training, adoption strategies, and measurement of expected outcomes.
  • Promote effective process management and digital ways of working across CMC Regulatory Affairs by sharing tools, methodologies, lessons learned, and scalable approaches.
  • Understand the business value of diverse teams, model inclusion, and embed the value of diversity in how teams are supported and led.
  • Understand employees’ skills, experiences, aspirations, and potential, and provide feedback, coaching, and insight to support their continued development.
  • Connect teams to broader organizational goals and purpose, provide support to remove barriers, and strengthen connections across the organization.

Desired Qualifications

  • A Bachelor of Arts or Bachelor of Science degree in Life Sciences, Engineering, or a related field, with relevant industry experience of at least 10 years with a Bachelor of Arts or Bachelor of Science degree, or at least 8 years with a Master of Science, Master of Arts, or Master of Business Administration degree.
  • Experience with CMC regulatory processes.
  • Experience with enterprise platforms and tools such as Veeva Vault, Planisware, Signavio, Visio, Power BI, or similar technologies.
  • Lean, Lean Six Sigma, or other process improvement training or certification; practical application of process improvement methodologies is more important than certification alone.

About the Company

Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Gilead Sciences is a biopharmaceutical company that discovers, develops and sells medicines for HIV, viral hepatitis and other liver diseases, cancer and inflammatory conditions. Its HIV business covers both treatment, led by the once-daily pill Biktarvy, and prevention, including Descovy and Yeztugo, a lenacapavir injection given twice a year. In cancer, its Kite unit makes CAR T-cell therapies from patients' own immune cells, and Trodelvy is an antibody-drug conjugate for breast cancer. Gilead earns revenue by selling its drugs to wholesalers, specialty pharmacies, hospitals and governments worldwide after regulatory approval. The company was founded in 1987 and is headquartered in Foster City, California.

Company size
10,001+
Company stage
IPO
Headquarters
Foster City, CA
Founded
1987

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