✦ Luna Orbit — IT Support & Helpdesk

Sr Manager, IT Business Analysis

at Gilead Sciences

📍 United States - California - La Verne Unknown 💰 $153K – $199K USD / year Posted March 13, 2026
Salary $153K – $199K USD / year
Type Not Specified
Experience mid
Exp. Years Not specified
Education Not specified
Category IT Support & Helpdesk

This role involves acting as the primary IT Business Analysis partner supporting manufacturing, quality, and digital initiatives at Gilead's La Verne site, focusing on process improvements, AI enablement, and regulated system support.

  • Serve as IT Business Analysis partner for manufacturing and quality
  • Drive process improvements and compliance
  • Support AI literacy and digital workflows
  • Manage validation and UAT activities
  • Collaborate with cross-functional teams

Supports GxP systems including MES, SAP, Veeva QMS, and automation interfaces, with a focus on compliance, validation, and digital workflows in a pharmaceutical environment.

The ideal candidate is a mid-level IT Business Analyst with experience supporting GxP regulated systems, process improvement, and digital enablement in a pharmaceutical manufacturing environment. Strong communication and collaboration skills are essential.

Business AnalysisGxP systemsrequirements gatheringprocess mappingUser Acceptance Testing
AI literacyAI-enabled use casesautomation interfacesGMax
SAPVeeva QMSGMaxMES
Business AnalysisAI literacyAI-enabled use casesMESSAPautomation interfacesVeeva QMSGMaxGxP systems21 CFR Part 11Good Documentation Practicesrequirements gatheringprocess mappingvalidation planningUser Acceptance TestingUAT
Business AnalysisAI literacyAI-enabled use casesMESSAPautomation interfacesVeeva QMSGMaxGxP systems21 CFR Part 11Good Documentation Practicesrequirements gatheringprocess mappingvalidation planningUser Acceptance TestingUATcross-site harmonization
communicationleadershipcollaborationproblem-solvingdecision support
Industry Healthcare IT
Job Function Business analysis and digital system support for pharmaceutical manufacturing and quality systems
Business AnalysisAI literacyAI-enabled use casesMESSAPautomation interfacesVeeva QMSGMaxGxP systems21 CFR Part 11Good Documentation Practicesrequirements gatheringprocess mappingvalidation planningUser Acceptance TestingUATvalidation

Lack of experience with GxP systems, No background in pharmaceutical or regulated industries, Inability to support validation and compliance activities

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