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 d
- oDossier preparation support: Assist the RA team with product life cycle submissions, including post‑approval variations, ensuring completeness and accuracy
- .Artwork review: Perform artwork proof‑reading prior to implementation to ensure regulatory conformity and version control
- .Project assistance: Contribute to product divestment activities (if applicable), following internal procedures and timelines
- .Document management: 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 admin: Provide operational and administrative support for assigned RA projects and meetings
- .Ad‑hoc tasks: Take on additional projects as assigned during the internship
.
What you will learn (learning outcom
- e)Regulatory framework: Understanding of Singapore's regulatory pathways for therapeutic product registration and post‑approval managemen
- t.HSA requirements: Practical insights into HSA guidelines, submission components, and life cycle management expectation
- s.Professional development: Strengthen technical, analytical, and communication skills through hands‑on assignments, shadowing RA personnel during submissions, and collaborating with cross‑functional stakeholder
s.
Internship Deta
- ilsInternship Duration: 5-6 mon
- thsStart Date: Urgent hire — candidates must be available to commence in June 2026/July 2
- 026Location Eligibility: Applicants must currently reside in Singapo
- re.Documentation Requirements: Applicants must possess the required internship support letter from their respective schools, as well as a valid student pass, where applicab
le.
