IT Solution Design Expert (Regulatory Affairs) Job ID REQ-10018836
Location: Barcelona (Hybrid / Office)
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Summary We are looking for an IT Solution Design Expert to join our Regulatory Affairs team. In this role, you will be responsible for leading the design and management of business critical applications in the RA Publishing domain. You will also provide support for applications from other domains that utilize Publishing data.
Purpose of the role:
Lead the design and management of RA Publishing business critical applications and provide support for applications from other domains using Publishing data.
Design and deploy Systems in the RA publishing domain which meet Business requirements. Collaborate with Business Users and Admins on future and current demand and keep current on Vendor and Health Authority roadmaps.
Provide hands-on management for development and support of applications in RA Publishing area and wider Operations domain.
Ensure development runs smoothly, drive continuous process improvement, and cooperate with various teams along the solution delivery value chain. Interact with all relevant stakeholders to ensure successful solution delivery with standard designs in line with industry best practices.
Major accountabilities: Design and manage the development of modular, reusable, elegantly designed, and maintainable software or solutions that support the RA organization as well as other Cross Functional strategic initiatives.
Participate in fit-gap workshops with business providing effort estimates and solutions proposals.
Hands-on, solution-driven, and customer-focused. Develop and maintain the code repositories for which you are responsible and respond rapidly to bug reports or security vulnerability issues.
Embody and integrate software development best practices into your everyday work and inspire others within the engineering community to emulate these practices.
Collaborate extensively with colleagues across Security, Compliance, Engineering, Project Management, Product Management, Product Service Management, and Business Management.
Continue support for moving Publishing other RA platforms to the cloud.
Ensure delivered solutions adhere to architectural and development standards, best practices, and meet requirements as recommended in the architecture handbook.
Ensure designed solutions are aligned with Data and Analytics strategy standards and roadmap. Bring innovations to the solutions and add measurable values to RA Business.
Commitment to Diversity & Inclusion We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum Requirements: University degree in Information Technology, Computer Sciences, Life Sciences or similar.
10+ years of IT technology development experience, preferably with 5+ years of experience working with Pharma Regulatory affairs (RA) business.
Experience working with RA Publishing business is a plus.
Strong technical background with large scale projects on technology like JAVA/.net, Oracle, MS SQL, IIS webserver, PowerShell or similar end-to-end technical solution delivery.
Experience on Publishing solutions like TRS, EFT and DMZ Gateway is preferred but not mandatory.
Familiarity with concepts of data and system security and compliance in highly regulated environments.
Languages:
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!
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