Regulatory Affairs Intern

Join our Regulatory Affairs team for an internship that provides structured exposure to the regulatory management of therapeutic products across their lifecycle. In this role, What you’ll do Dossier preparation suppor t: Assist the RA team with product life cycle submissions, including post‑approval variations, ensuring completeness and accuracy Artwork revie w: Perform artwork proof‑reading prior to implementation to ensure regulatory conformity and version control Project assistanc e: Contribute to product divestment activities (if applicable), following internal procedures and timelines Document managemen t: Maintain and organize regulatory files (electronic and paper) for reliable tracking, retrieval, and archiving of controlled documents Good Regulatory Practice (GRP ): Support GRP activities and routine compliance checks to align with internal SOPs and HSA expectations Operations and admi n: Provide operational and administrative support for assigned RA projects and meetings Ad‑hoc task s: Take on additional projects as assigned during the internship What you will learn (learning outcomes) Regulatory framewo rk: Understanding of Singapore’s regulatory pathways for therapeutic product registration and post‑approval management HSA requiremen ts: Practical insights into HSA guidelines, submission components, and life cycle management expectation Professional developme nt: Strengthen technical, analytical, and communication skills through hands‑on assignments, shadowing RA personnel during submissions, and collaborating with cross‑functional stakeholders Internship Details Internship Duration: 5-6 months Start Date: Urgent hire — candidates must be available to commence in Jul/Aug 2026 Location Eligibility: Applicants must currently reside in Singapore Documentation Requirements: Applicants must possess the required internship support letter from their respective schools, as well as a valid student pass, where applicable