Ruban Joseph Email & Phone Number

England, United Kingdom

Staffordshire, England, United Kingdom

Macclesfield, England, United Kingdom

• Lead elements of the solution architectures within the Pharmaceutical Development and Quality portfolios, contributing to the solution architecture principles.
• Work closely with the client, Project Managers, and technical teams to ensure that each system is built and updated to meet the needs of the protocol.
• Achieved successful execution of application lifecycle retirement (decommission, execution and benefits realisation.
• Designed various RIM solutions achieving high standards in efficiency and reducing downtime.
• Provided Efficient solutions for regulatory information management (RIM) capabilities including data and document management, submission publishing and archival on a single cloud-based platform
• Taking ownership of critical incidents, coordinating with resolution parties, and establishing effective communication between stakeholders for post-incident reviews. Achieved a reduction in downtime by about.

India

• Successfully used the Veeva Platform to manage crtitical Marketing related documents.
• Responsible for the System configuration and system administration of the Veeva PromoMats system.
• Ensure teams are developing reliable regulatory content with high data integrity.
• Understand the business processes (across R&D and Manufacturing), regulatory and reporting requirements and converting these into RIM configuration ideas/proposals
• Define strategies and implementation programs for deploying Veeva Vault RIMS across the Platform.
• Develop and deliver data and document migration strategies.

United Kingdom

• Deputed to a leading UK based Pharmaceutical company in Uk for analyzing the functioning of various regulatory lifecycle process and understanding end user requirements on the platform
• Successful execution of AZDoc Migration Project, migrating document management systems to a new platform, affecting over 2,000 users across 3 continents. Achieved a 98% customer satisfaction rate during the transition.
• With Strong understanding of GxP and Lifesciences processes, ensured that the documents are meeting the quality standards, and the product meet the strict quality standards during the entire process of production.
• With the expertise in EDMS/RDMS, successfully ensured the activities like maintenance of document lifecycle, better management of documents for improved submission-readiness. This has made Business achieve the goals.

India

• Lead the Vaccine Project, allowing users to report the issues about vaccine using a global web Application.
• Achieved high-quality user-friendly web portal using integration technologies like MULESOFT.
• Responsible for implementing critical components and resolving complex technical challenges.
• Leading in hands-on coding, code reviews, and troubleshooting to guide the team in building high-quality software applications. (in C#)
• Ensured timely delivery by delegating tasks and setting clear team goals, continuous improvement meetings.
• Successful in bridging the gap between the business and the technology, helping to translate business requirements to the team and vice versa, communicate technical challenges and limitations to the business.

India

• Led a team in maintaining and supporting critical IT platforms, focusing on reliability and performance.
• Worked on various development, re-engineering, platform services maintenance, and support projects in the Life Sciences domain.
• Coordinated with internal teams and external vendors to resolve incidents and improve overall service quality.

• Collaborated with cross-functional teams to support and maintain business-critical applications, adhering to ITIL best practices.
• Assisted in the delivery of managed IT services, ensuring compliance with GxP regulations.
• Developed and implemented processes to improve system stability and reduce incident frequency.

Bachelor Of Engineering (Beng)

Computer Sciences

Education record

Education record