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Associate Director DDIT Dev.IT PS&PV Science, GC&T TDE
2 years ago
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Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us!
About the Role: Create the detailed DDIT solution/service design, based on functional specifications to meet quality and performance requirements and technical constraints. Responsible for detailed design, development, and delivery of system solutions for Safety Science, Governance, Communication & Training
- Create the detailed process designs necessary to operate the software/service on a day to-day basis
- Ensure designs produced adhere to architectural roadmap and support the development, execution, and operations of software/service
- Peer review and sign off detailed designs by business.
- Ensure that detailed designs adhere to solution architecture design (i.e. high level conceptual design) and are traceable to functional as well as non-functional requirements in functional specification
- Ensure the overall user experience is considered when designing new solutions and services
- Take accountability to ensure adherence with Security and Compliance policies and procedures within Service Delivery scope.
- Provides comprehensive and authoritative technical or professional guidance on a wide range of issues within the area of project execution to influence internal and/or external stakeholders
- Create, maintain, and iterate on our CI/CD processes for new and existing services
Education:
- Bachelor’s degree in Computer Science, Computer Engineering or related technical discipline or equivalent experience demonstrated
Experience:
- 10+ years of experience with expert understanding and proven track record in analyzing business processes, architecting, designing, developing and/or integrating complex, cross-divisional end to end solutions with large data volumes
- Experience in integrating Commercial off-the-shelf products such as Oracle Argus Safety, Empirica or Safety reporting solutions is strongly desired
- Excellent verbal and written communication skills with ability to interact with senior stakeholders within the Patient Safety global function.
- Self-starter with ability to work autonomously in a highly matrixed and multi-cultural environment, taking full ownership of deliverables.
- Experience in highly regulated environments, ideally Drug Development within the Pharma industry, including Computer System Validation, preferred
- Experience in Agile project implementation would be a plus