Protégé – Regulatory Affairs (12 months)

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We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Non-Standard

Job Sub Function:
Non-Employee

Job Category:
Non-Standard

All Job Posting Locations:
Petaling Jaya, Selangor, Malaysia

Job Description:

We are searching for the best talent for Protégé - Regulatory Affairs

Purpose:

The Protégé - Regulatory Affairs will support the local Regulatory Affairs team in Malaysia, contributing to regulatory activities across assigned product portfolios.

This role provides a structured learning experience to develop foundational regulatory knowledge, ensuring compliance with local health authority requirements while supporting timely product registration and lifecycle management.

You will be responsible for:


* Supporting the preparation and submission of regulatory applications for product registration, renewal, and variations in accordance with local regulatory requirements


* Maintaining and updating internal and source company regulatory databases to ensure accuracy and compliance


* Liaising with global and regional regulatory teams to obtain required documentation and ensure alignment with Malaysia regulatory requirements


* Coordinating with local health authorities by compiling submissions and supporting responses to regulatory queries


* Assisting in tracking regulatory timelines and ensuring timely execution of submission plans to support product availability


* Participating in cross-functional discussions to understand business needs and align regulatory strategies accordingly


* Contributing to team meetings, sharing learnings, and gaining exposure to regulatory best practices and processes


* Supporting ad hoc regulatory activities and projects as assigned by the Regulatory Affairs Manager

Qualifications / Requirements:


* Bachelor's degree in Life Sciences, Pharmacy, or a related discipline


* Strong interest in Regulatory Affairs and the pharmaceutical or healthcare industry


* Good understanding of basic scientific principles and healthcare product lifecycle is an advantage


* Strong attention to detail with the ability to manage documentation accurately and systematically


* Good organisational and time ma...