Systems, Engineer IV - eQMS DD&T
Takeda Pharmaceutical Company Limited (company site, opens in a new tab)5+ yrsBengaluruOn-siteDirect career pageEst. 18–32 LPA
Posted 21h ago
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Job description
Structured overview of role & requirements
About This Role
- Own end-to-end lifecycle of eQMS products including strategy, development, release, support, and continuous improvement across global multi-site GxP environments.
- Lead Veeva Vault QMS technical activities ensuring compliance with regulations (21 CFR Part 11, EU Annex 11, data integrity), validation, and audit readiness.
- Manage stakeholder relationships, product budgets, vendor contracts, and technical support operations to maintain system stability and deliver value aligned with business needs.
Minimum Requirements
- Bachelor's degree or equivalent in scientific discipline, computer science, or business administration (Master's preferred).
- Minimum 5 years of relevant professional experience including IT service delivery or pharmaceutical product management.
- Experience with regulated systems including GxP compliance and system validation standards.
- Work Experience Required: 5+ years in related fields
Ideal Candidate Profile
- Experienced in managing complex, regulated SaaS quality platforms, ideally in pharmaceutical life sciences.
- Strong stakeholder and vendor management skills with ability to influence cross-functional global teams.
- Proficient in Agile Scrum, design thinking, and driving product strategy and delivery in a virtual/global environment.