Senior Business Analyst - Pharmaceutical Industry
CapgeminiAbout the role
Choosing Capgemini means choosing a company where you will be empowered to shape your career in the way you’d like, where you’ll be supported and inspired by a collaborative community of colleagues around the world, and where you’ll be able to reimagine what’s possible. Join us and help the world’s leading organizations unlock the value of technology and build a more sustainable, more inclusive world.
About the Job You're Considering
Join Capgemini as a Senior Business Analyst to drive business outcomes for a new initiative to enable compliant, high-quality experimentation. As a partner to product management, engineering, data, QA, compliance, and vendor teams, this role will translate complex scientific and operational needs into clear requirements, orchestrate end-to-end process and data design, and ensure value realization from a COTS/SaaS platform in a regulated environment. The ideal candidate brings deep business analysis expertise across life sciences/CMC workflows, strong experience with commercial platforms, and fluency working in SAFe/Agile-at-scale programs.
Location
This is a hybrid role located in Gaithersburg, MD. Remote work is permitted, with an in office requirement of 2-3 days per month.
Your Role
- Partner with product/program management, engineering, data, QA, compliance, and vendor teams to gather and clarify business, scientific, and operational needs.
- Translate complex CMC/experimentation workflows into clear, testable functional and non-functional requirements and user stories.
- Define data models, interfaces, and information flows needed to enable compliant, high-quality experimentation.
- Lead/coordinate implementation of new COTS and SaaS solutions aligned to regulatory requirements. Configure capabilities, define integrations, and align platform features to business outcomes.
- Establish success metrics/KPIs and ensure value realization from the platform and workflows.
- Support backlog prioritization, release planning, and readiness (incl. change management and training inputs).
- Ensure processes and requirements align with applicable GxP/QA and data integrity expectations. Partner with QA/compliance to embed controls, auditability, and validation considerations.
- Leverage SAFe methodology and ceremonies (PI planning, backlog refinement, sprint reviews), and maintain high-quality artifacts (epics/features/stories, acceptance criteria) to support User Acceptance Testing.
- Coordinate with vendors on solution design, issues, and roadmap alignment. Communicate status, risks, and decisions to cross-functional stakeholders.
Your Skills and Experience
- 5+ years of documented experience in a business analyst or PMO role in pharmaceutical or life sciences organizations.
- Hands-on experience implementing or working with commercial (COTS/SaaS) platforms—ideally in laboratory, bioprocess, or experimentation domains.
- Demonstrated delivery within regulated environments with QA/compliance collaboration.
- Practical experience working in SAFe/Agile-at-scale programs
- Familiarity with validation, data integrity, and GxP considerations for SaaS/COTS implementations.
- Strong understanding of CMC/life sciences workflows and associated data/process needs.
- Excellent stakeholder management, facilitation, and communication skills.
Job Description - Grade Specific
Is fully competent in its own area and has a deep understanding of related programming concepts software design and software development principles. Works autonomously with minimal supervision. Able to act as a key contributor in a complex environment, lead the activities of a team for software design and software development. Acts proactively to understand internalorexternal client needs and offers advice even when not asked. Able to assess and adapt to project issues, formulate innovative solutions, work under pressure and drive team to succeed against its teApply for this role
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