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Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Manager – IT Quality Engineering

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeFoster City, CA, USA

About the Job

Requirements

  • Six or more years of experience with a bachelor's degree, or four or more years of experience with a master's degree.
  • Computer Science or a related discipline is preferred.
  • Specific experience in the life sciences, pharmaceutical, medical devices, or healthcare industries.
  • Strong knowledge of global regulatory requirements such as GMP, GCP, GLP, GDP, or other domains.
  • Strong background and management experience in validation.
  • Significant experience leading validation across multiple projects, supporting GxP assessments, estimating schedules, resources, and tasks, and managing escalations and dependencies.
  • Experience validating SAP ERP, supply chain, LIMS, manufacturing, Salesforce, Veeva, or patient safety applications is a plus.
  • Hands-on experience managing requirements and test artifacts in requirements and test management tools such as Application Lifecycle Management (ALM).
  • Strong experience managing complex data migration projects and supporting development of data migration plans and strategy.
  • Strong experience validating end-to-end integrations built with various integration solutions.
  • Strong experience managing change controls, Corrective and Preventive Actions (CAPAs), and deviations.
  • Strong experience with managed service operations.
  • Hands-on experience in software quality assurance and ability to influence stakeholders to apply software testing standards in the software development life cycle.
  • Strong collaboration skills to work effectively with leaders, managers, and subject matter experts.
  • Knowledge and experience with Computer Software Assurance (CSA).
  • Ability to track and follow up on actions requiring team completion.
  • Ability to lead and influence cross-functional teams, global site employees, and functional-area employees toward successful project outcomes.
  • Ability to provide a clear perspective and rationale and function successfully in a dynamic environment.
  • Strong experience troubleshooting complex system and application quality and compliance issues and recommending appropriate remediation.
  • Significant experience supporting IT integrations and transformations in a corporate or other relevant business environment.
  • Experience supporting IT quality and compliance audits and inspections.
  • Significant experience managing IT consultants and vendors.
  • Coaching and collaboration skills to interact with personnel at all levels to achieve shared goals.
  • Ability to develop and maintain effective relationships with internal and external stakeholders.
  • Ability to lead and influence onshore and offshore development and validation teams.
  • Knowledge and experience with continuous integration and continuous delivery (CI/CD) deployment methods, source code management, and DevOps tools.
  • Working knowledge of Waterfall, Scrum, DevOps, and Agile methodologies.
  • Broad understanding of development and test management tools, including Micro Focus ALM, Jira, and Azure DevOps.

Responsibilities

  • Work closely with business leads and other IT partner functions to develop and maintain an in-depth understanding of business needs and objectives in business and technology.
  • Stay abreast of changes in assigned business and technology areas to proactively recommend future solutions and opportunities.
  • Support validation of regulated system implementations, audits, and inspections.
  • Oversee a complex portfolio of systems and ensure validation activities adhere to quality standards and best practices.
  • Manage an area of the overall IT Quality Engineering Program that impacts multiple business areas or geographies.
  • Strategically manage validation activities across multiple projects and portfolios, including AI initiatives, to align with business goals and maximize validation efficiency.
  • Oversee and provide guidance to IT Quality Engineers supporting multiple projects.
  • Use Gilead test management tools hands-on and apply the underlying processes and best practices to manage validation artifacts and deliverables.
  • As a validation subject matter expert, review or approve specifications, protocols, change controls, Corrective and Preventive Actions, and deviations to ensure compliance with Gilead procedures and applicable regulations.
  • Support implementation of short- and long-range strategies, plans, tools, and tactics for IT Quality Engineering and compliance.
  • Apply understanding of application development methods, project management processes, and fundamentals of requirements specification, design, and development/configuration.
  • Support and maintain IT Quality Engineering domain principles and practices to ensure quality and compliant delivery to the business.
  • Support development and implementation of the technology and process roadmap for the IT Quality Engineering domain.
  • Promote continuous improvement and learning across portfolios.
  • Work with peers and leads to identify opportunities and implement changes that improve validation process efficiency.
  • Evaluate activities and deliverables to ensure results align with Gilead requirements and metrics needs.
  • Manage escalations and participate in project teams as required.
  • Monitor metrics to proactively detect trends and assess testing effectiveness.
  • Maintain awareness of industry best practices and standards.

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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