IT SOLUTION DESIGN EXPERT (REGULATORY AFFAIRS)

Summary Location.
Barcelona (Hybrid / Office) Novartis is unable to offer relocation support for this role.
please only apply if this location is accessible for you.
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.
The purpose of the role is to.
• Lead the design and managing deliverables of RA Publishing business critical applications as well as 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, 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.
Usual stakeholders are Application Owners, Delivery Managers, Architecture teams, Data Scientists, DevOps, Security, Integration Factory, Infrastructure teams, Platform Support teams, ISRM team as well as Product Owners About the Role Major accountabilities.
Design and manage the development of modular, reusable, elegantly designed and maintainable software or solutions that supports the RA organization as well as other Cross Functional strategic initiatives.
Participate 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 your 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 experience in IT technology development experience, preferably with 5+ years of experience working with Pharma Regulatory affairs (RA) business.
Experience working in with RA Publishing business is a plus.
Strong technical background with large scale projects on technology like JAVA/.
et, 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.
English.