Product Manager leading Rivian’s connected EV mobile app experience. Owning strategy, app coherence, quality, and end - to - end delivery across mobile and vehicle software.
About the role
- Roche Product Owner leading Veeva QMS technology, data governance, and lifecycle management. Improving compliant quality systems across global pharmaceutical manufacturing and commercial sites.
Responsibilities
- Oversee large-scale, cross-functional systems, including dependencies, integrations, and long-term planning
- Lead multiple products or complex technologies through system lifecycle management, including change management
- Influence future innovation through interdepartmental and industry collaborations
- Translate complex business use cases and requirements into standardized, compliant technology solutions
- Champion cross-functional collaboration and alignment across internal and external stakeholders
- Identify opportunities to leverage technology innovations to improve business efficiency and outcomes
- Drive integration of technology-driven solutions in a competitive and changing industry landscape
- Initiate, manage, and close complex deviations, CAPAs, or changes; support audits and regulatory inspections
- Define and monitor KPIs for IT system and product performance, efficiency, and user satisfaction
- Serve as global Principal Product Owner for QMS technologies, especially Veeva Quality Vault QMS and potentially Veeva Quality Docs
- Manage Veeva QMS and Quality Docs ecosystem integrations, data flow, reporting, and interface connectivity across global manufacturing and commercial sites
- Direct system lifecycle activities, including upgrades, replacements, and retirements, while following change management processes
- Partner with business stakeholders and IT to define product vision, align roadmaps, manage backlogs, and prioritize enhancements
- Act as Business Data Steward, ensuring GxP compliance, data governance, and adherence to global quality policies
- Mobilize and lead cross-functional teams across global functions, sites, IT partners, and validation functions
Requirements
- 12+ years of experience in Veeva Quality Vault or equivalent Quality platform management, ideally Veeva QMS and Veeva Quality Docs
- Bachelor’s or Master’s degree in Life Sciences, Computer Science, or a related field, or an equivalent qualification like a Federal Diploma of Higher Education
- Proven track record in formulating long-term computer system strategies
- Strong understanding of data integrity, data analytics, and software validation within validated or controlled pharmaceutical/healthcare environments
- Knowledge of GMP, FDA, and GxP requirements
- Skilled in Agile methodologies
- Exceptional communication skills for conveying technical findings and recommendations to technical and non-technical audiences
- Technical foundation and business acumen to troubleshoot intricate system issues, navigate escalation paths, and adapt setups to diverse site-specific needs
- Must work in a regulated pharmaceutical/healthcare environment and support GxP-compliant systems and processes
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