Monitor and summarize regulatory updates from global health authorities (e.g., FDA, EMA, TGA, ANVISA, SFDA).
Assist in categorizing regulatory changes by industry, product type, jurisdiction, and topic (e.g., labeling, clinical trials, pharmacovigilance).
Draft concise summaries and impact assessments for new regulations, guidance documents, and enforcement actions.
Support the maintenance of RegASK’s regulatory databases and internal knowledge repositories.
Collaborate with regulatory experts and analysts to ensure data accuracy and relevance.
Help prepare reports and dashboards for client deliverables and internal use.
Contribute to the optimization of workflows and AI-supported tools for regulatory monitoring.

Currently pursuing or recently completed a degree in Life Sciences, Pharmacy, Public Health, Regulatory Affairs, or a related field.
Strong analytical and research skills with attention to detail.
Excellent written and verbal communication skills in English.
Interest in regulatory science, compliance, and emerging technologies such as AI and data analytics.
Ability to work independently in a fast-paced, collaborative, and multicultural environment.
Previous experience or coursework related to regulatory affairs, quality assurance, or compliance is an advantage.

Exposure to real-world regulatory challenges across multiple industries and regions.
Hands-on learning at the intersection of AI, SaaS, and Regulatory Intelligence.
Mentorship and professional development opportunities with industry experts.
A dynamic, fast-growing environment where your contributions make a visible impact.

RegASK™

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