RA Specialist

Johnson & Johnson is currently seeking a RA Specialist located in Singapore.

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at https://www.jnj.com/

Position Summary

As a RA Specialist, coordinates, compiles, and submits applications of new products or changes to the approved products to the regulatory agencies.

Ensures compliance with regulatory agency regulations and interpretations.

Prepares responses to regulatory agencies' questions and other correspondence.

Gathers and assembles information necessary for submissions in accordance with regulations and relevant guidelines.

Involved with the preparation of necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides.

Provides solutions to a variety of problems of moderate scope and complexity.

Organizes and maintains reporting schedules of new product registration, changes in products, projects, etc.

As an APJ Veeva Coordinator, primary responsibility is to ensure the smooth operation and effective use of the Veeva system within the organization.

The Veeva system is a copy clearance approval system for advertisement and promotional material, and local labelling materials in Johnson & Johnson Vision.

In this role, you will be responsible for managing and coordinating various aspects of the Veeva system to support sales, marketing, and regulatory activities.


* Responsible for APJ Vision advertisement and promotional materials, and local labelling materials.


* Ensure the smooth operation and optimal utilization of the VEEVA system while managing and coordinating various aspects of the VEEVA system to support APAC Vision advertisement and promotional materials, and local labelling.


* Ensure compliance to applicable JJV Copy Approval procedure(s)

Enhancing efficiency, establishing streamlined procedure(s), and integrating the Vision procedure(s) will be the key focus areas through the APAC copy review and labelling approval process project.

Responsibilities:

VEEVA Coordinator


* System Administration/Coordination: Serve as the main point of contact for Veeva system administration/Coordination, including user access management, security settings, and configuration updates.


* User Support and Guide/Training: Provide support for Veeva system users, including troubleshooting issues, answering inquiries, and conducting training sessions to ensure proper system utilization.


* Data Management: Oversee the accuracy and integrity of data within the Veeva system, including data entry, data maintenan...