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Job Description
The Sr IT Business Analysis Specialist (Tech Dev Biologics Clinical Manufacturing) in the PDM IT organization will be a strategic technology partner to the PDM Biologics Clinical Manufacturing business capability working with business colleagues to align technology direction with business goals and help define relevant and effective solutions while maturing existing systems and services in order to drive business value.
The Sr Specialist will be responsible for the ideation planning development oversight for the Biologics Clinical Manufacturing business capability. Participates in short and long-term business or IT strategic planning sessions identifying opportunities and making recommendations for the enablement of capabilities. Participates in the analysis efforts for business case development including resource estimates prioritization and categorization. Advises on options risks costs versus benefits and impacts on end-user processes and system priorities. Engages and collaborates with business leadership team members senior business stakeholders and business process owners to cultivate technology solution aligning with business or IT strategies. Establishes and maintains a strategic relationship with leadership team members and senior business stakeholders.
The role will be involved with IT solutions planning for PDM Digital Strategy initiatives through to successful execution of these initiatives. Projects may include web-based solutions (SaaS) specialized Tech Dev Biologics Clinical Manufacturing applications extending enterprise technologies and supporting IT Operations and Solution Delivery teams to enhance business effectiveness. Critical to the role will be championing projects and working with business teams to prioritize across initiatives. Also works with Technical Development IT leadership in assisting in the management of the application portfolio. This role will direct both internal and a significant contingent of managed and contracted services staff to drive business outcomes.
Cultivates and demonstrates a working knowledge of Biologics Clinical Manufacturing Facilities & Engineering and Quality Control.
Participates in short- and long-term strategic planning session to improve business or IT processes through capability development
Participates in discovery sessions to identify opportunities for improvements in business capabilities or IT operations and formulate proposals for cost-effective solutions based on engagement project and operations activities
Demonstrates how capability enablement can assist selected departments / business areas and how platforms and solutions can support the achievement of short- and long-term business or IT capability goals
Establishes and maintains a strategic relationship with select functional level stakeholders based on experience and contribution to business operations
Participates in the development of business use cases cost structure and ROI model in support of investment projects and activities to build IT Roadmap and demonstrate clarity on how solution provides business value
Actively communicates with select business capabilities IT vendors and other stakeholders to ensure awareness of vision roadmap progress risks and results associated with a key capability
Works with appropriate business Subject Matter Experts (SMEs) and business stakeholders to proactively identify and evaluate risks associated with business decisions that may impact a capability enablement
Participates in workshop sessions for incremental roadmap assessments and business alignment
Educates and aligns business digital vision and needs with IT initiatives beyond technical feasibility
Illustrates contextual insight to ensures IT development supports revenue growth compliance and customer outcomes
Presents Voice of the Business by capturing evolving business needs and translates them into system capability targets
Participates in workshop sessions for Strategic Planning to connect business objectives to long-term IT capabilities
Provides input to anticipates changes in scale market or regulation to future proof and incorporate them into the roadmap
Participates in cross-functional teams to align product operations and IT on a single direction
Provides input to Business Translation Layer to ensure delivery solves business problems to enable DevOps team for code delivery
Reduces rework by validating business requirements upfront avoiding costly misalignment during implementation
Enhances change management with increased adoption by ensuring workflows and training match the business context
Works with business process owners and DevOps leads to cultivate appropriate solution required to meet business or IT objectives
Engages Domain Architecture team to align long-term technology strategy with business objectives
Sets proper expectations with business and supports escalation and resolution through negotiation or governance mechanisms
Participates in analysis of current and future technology trends to determine impact to the business provides input to IT team lead to promote capability enablement and benefit realization
Communicates to other IT domains for awareness of key capability aspects how they operate and how they are impacted
Participates in tracking business KPIs post-implementation
Provides feedback loops for product enhancements and roadmap updates
Provides input to ensure IT delivery remains aligned with evolving business needs
Provides input to IT team lead to help prioritize the flow of work in program backlog
Fosters a team environment and shares relevant information with IT team members
Strong communication excellent research skills and learning agility to understand internal business or IT process best practices and translate into technology needs/opportunities
Strong collaboration stakeholder management and communication skills including verbal written and negotiation
Strong Listener. Be able to patiently listen to understand the business needs
Strong work ethic a sense of business urgency and the ability to work effectively with many deadlines in a complex matrix organization
Proven track record of critical thinking analytical ability operational excellence and detail orientation.
Possesses ability to analyze make critical decisions based on analysis
Ability to find innovative ways to resolve problems
Experience in stakeholder management dealing with middle management up to executive level
Specific experience in the Life Sciences/Pharma/Medical Devices/Healthcare industries is preferred
Demonstrated expertise in technology environments relevant to Biotech Clinical Manufacturing production
Experience with platforms critical to Biologics Clinical Manufacturing (e.g. MES / Electronic Batch Records ERP Mfg CMMS Digital Process and Automation Historian IOT etc. ) and a willingness to learn and adapt to new Biologics Clinical Manufacturing IT systems as they emerge
Extensive knowledge of Agile methodologies and tools (e.g. Jira Asana etc.) with proven abilities to apply these in supporting IT solutions that meet both business needs and clinical manufacturing objectives.
Experience in programming environments (e.g. Python R) and cloud computing platforms (e.g. AWS) especially those relevant to data and analytics in life sciences is very desirable
Awareness of emerging IT trends and technologies (e.g. GenAI Digital Twin Process Analytical Technology AI/ML Predictive Analytics etc.) with a commitment to continuous learning especially in areas relevant to biopharmaceutical research.
Bachelors degree and 5 years of relevant experience; OR
Masters degree and 3 years of relevant experience
Degree in computer science information sciences or related field or equivalent experience.
Strong understanding of GxP compliance and 21 CFR Part 11 requirements.
Significant IT experience in a corporate or other relevant business environment with a strong preference for experience in the biopharmaceutical industry.
Experience with IT implementations integrations cloud transformations and understanding of data security and compliance issues in a scientific or healthcare setting.
Knowledge of Biologics Clinical Manufacturing processes
Highly organized results-oriented and attentive to details self-motivated proactive independent and responsive - requires little supervisory attention
Good understanding of GxP compliance and 21 CFR Part 11 requirements
Experience with Biologics Clinical Manufacturing is preferred
Must be quality oriented and ensure all work streams are aligned with business IT compliance and cGMP regulation
Ability to translate technical topics into business terms
Create Inclusion - knowing the business value of diverse teams modeling inclusion and embedding the value of diversity in the way they manage their teams.
Develop Talent - understand the skills experience aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow develop and realize their purpose.
Empower Teams - connect the team to the organization by aligning goals purpose and organizational objectives and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.
For additional benefits information visit:
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment and is dedicated to fostering an inclusive work environment comprised of diverse perspectives backgrounds and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race color religion national origin sex age sexual orientation physical or mental disabilitygenetic information or characteristic gender identity and expression veteran status or other non-job related characteristics or other prohibited grounds specified in applicable federal state and local order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973 the Vietnam Era Veterans Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990 applicants who require accommodation in the job application process may contact for assistance.
For more information about equal employment opportunity protections please view theKnow Your Rights poster.
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YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
Please apply via the Internal Career Opportunities portal in Workday.
Required Experience:
Senior IC
Gilead Sciences is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensu ... View more