Business Analyst
Katalyst Healthcares and Life Sciences - Philadelphia, PA
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Job Summary: The Business Analyst (Integration) acts as a key interface between business and IT functions within a pharmaceutical environment. The role supports initiative scoping, business process harmonization, stakeholder communication, and integration of standardized data models, applications, and technologies in alignment with Informatics strategies and architectures. The position requires strong analytical skills, regulated (GxP/CSV) working knowledge, and the ability to collaborate across multiple business units and IT teams. Roles & Responsibilities: cts as an interface between business and IT functions and serves as a contact point for business leads to launch initiatives, leading and driving the scoping phase. Collaborates with IT Business Partners, Stakeholders, Product Owner, Solution Architect, CSV Lead, and SMEs. Strives for harmonization of business processes across sites and departments by propagating common standardized data models, applications, and technologies aligned with cross-functional or Informatics strategies and architectures. Performs detail-oriented work with a high degree of accuracy and explains complex concepts with clarity and simplicity. Demonstrates knowledge of current GxP requirements and documentation standards, including the ability to write validation documentation. Manages communications with multiple business units and internal IT cross-functional teams. pplies Agile working practices. Supports business partnering activities, including requirements elicitation and management, business process analysis and design, usability, and workshop facilitation. Demonstrates strong stakeholder management skills. Shows change management awareness with empathy for people on site. Education & Experience: Bachelor's degree (or equivalent experience) in Computer Science, Software/Electronics Engineering, Information Systems, or a closely related field. 3-5 years of experience as a Business Analyst in the pharmaceutical industry. GxP/CSV experience with a regulated way of working. Strong technological background in Manufacturing or QC environments (e.g., Empower, SoftmaxPro, DeltaV, Veeva as a Quality solution). One resource requires GMP experience; a second resource does not require GMP experience. Experience with global or multi-site manufacturing projects. Familiarity with Roche-internal project methodology. Fluent in English.
Created: 2026-03-04