Location : Barcelona #LI-Hybrid
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
This role's purpose is to act as a consultant and advisor, providing guidance to improve complex global business processes, products, and services. We are looking for an experienced individual in Global Drug Development Regulatory Affairs to lead technical activities for solutions that redefine how Novartis operates.
You will work on strategic initiatives with the mandate to deliver solutions that will bring transformative change to the business domain and enable Novartis to gain a competitive advantage.
About the Role
Role Responsibilities:
* Create detailed process designs necessary for the daily operation of software/services.
* Ensure designs adhere to the architectural roadmap and support development, execution, and operations.
* Ensure designs align with solution architecture and trace back to functional and non-functional requirements.
* Consider user experience when designing new solutions and services.
* Ensure compliance with security and policies within Service Delivery scope.
* Provide input on project proposals related to new technologies and innovations.
* Drive Proof of Concept activities; evaluate new technological standards and their application.
* Collaborate with project managers, workstream leads, and product squads to deliver roadmaps and participate in sprint planning.
* Coordinate with vendors and internal teams to ensure documentation and technical requirements are accurately interpreted and implemented.
* Act as a technical liaison between business and implementation partners.
Role Requirements:
* Bachelor's degree in engineering or pharmaceutical discipline; advanced degrees and certifications are a plus.
* 12+ years of IT solution architecture experience with strong communication skills.
* Proven knowledge of SDLC, Validation, and Compliance.
* Proficiency with tools such as Jira, Confluence, HPQC, and modeling tools.
* Experience in data migration and system integration projects.
* Experience managing GxP projects is desirable.
* Global experience interacting with senior management and collaborating across boundaries.
* Experience in Regulatory Affairs processes or Veeva Submission modules is a plus.
Why Novartis: Helping people with disease involves more than science; it requires a community of passionate individuals working together to achieve breakthroughs that change lives. We are committed to an inclusive, diverse work environment.
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