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 aims to act as a consultant and advisor, providing guidance to improve complex global business processes, products, and services. We are seeking an experienced individual in Global Drug Development Regulatory Affairs to lead technical activities for solutions that redefine Novartis's operations.
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 daily operation of the software/service.
* Ensure designs adhere to the architectural roadmap and support software/service development, execution, and operations.
* Ensure designs are aligned with solution architecture and traceable to functional and non-functional requirements.
* Consider user experience in designing new solutions and services.
* Ensure compliance with security and policies within Service Delivery scope.
* Contribute to project proposals for new technologies/innovations.
* Drive Proof of Concept initiatives and evaluate new technological standards.
* Collaborate with project managers, workstream leads, and product squads to deliver the product roadmap, participate in sprint planning, and ensure deliverables are on track.
* Liaise with vendors, internal IT teams, and business to ensure documentation and technical requirements are accurately interpreted and implemented.
* Serve as a technical expert 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 architecting experience with strong communication skills.
* Proven knowledge of SDLC, Validation, and Compliance.
* Proficiency with tools such as Jira, Confluence, HPQC, modeling tools.
* Experience in data migration and system integration projects.
* Experience managing GxP projects is desirable.
* Global experience interacting with senior management and influencing across boundaries.
* Experience in Regulatory Affairs processes or Veeva modules is a plus.
Why Novartis: Helping people with disease and their families requires more than science; it requires a community of passionate individuals. Join us to make a difference. Learn more.
We are committed to an inclusive, diverse work environment that reflects the communities we serve.
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