Summer Internship: GxP Surveillance Intern (Remote)

BeiGene

8d•$27 - $27•Remote

About The Position

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. Internship program dates: June 8 - August 21, 2026 Education Required: Bachelor’s degree in progress: Life Sciences, Pharmacy, Biomedical, Chemical engineering related degree General Description: Provide support to GxP Surveillance and GxP Intelligence Management System. Actively and meticulously monitoring regulatory GxP requirements and expectations. Daily screening and gathering new & changed regulations, guidance, trends, intelligence and regulatory enforcement activities with potential impact to BeOne products, processes and business in its priority markets. The source of regulatory / GxP Intelligence for daily screening are news organizations, subscription-based databases, scientific organizations such as PDA, ISPE, etc., Global Regulatory Agencies websites, International Organization websites e.g., ICH, WHO, PIC/S. Generation of daily reports for further assessment by the Triage Leads and subject matter experts from various GxP functions. Essential Functions of the Job: The regulatory surveillance on GxP (GLP, GCP, GVP, GMP, GDP/GSP, Pharmacopeia, Medical Device and Diagnostics, Drug-Device Combination product, Chemistry Manufacturing, Control (CMC), Supply Chain and Good AI Practice). Geographic coverage is Greater China, Central & South Asia (GCC&SA), North America (USA and Canada), Europe, Japan & Asia Pacific (JAPAC) and New Markets (Latin America, Middle East & North Africa, South Africa, Russia, Israel and Türkiye). Efficient web searing and source evaluation. Navigating regulatory authority websites (US FDA, EMA, PMDA, WHO, ICH, Pharmacopeia) Monitoring updates, guidance documents, health authority notifications, alerts, and public consultation documents. Document management – file organization and version control. Supervisory Responsibilities: NIL

Requirements

Bachelor’s degree in progress: Life Sciences, Pharmacy, Biomedical, Chemical engineering related degree
Basic computer skills – MS Office / Microsoft 365, Excel, PowerPoint, Outlook.
Collaboration Tools – MS Teams, SharePoint, OneDrive (basic use for the file sharing and collaboration).
Data Handling & Accuracy – Attention to detail in data capture and documentation.
Maintaining logs, trackers, and simple databases for regulatory surveillance.
Strong organizational skills
Ability to interpret, synthesize, and communicate information
English communication skills both written and oral
Ability to understand technical, scientific and medical information
Ability to prioritize, demonstrating good time management skills
Self-motivated, with the ability to work proactively using own initiative.
Committed to learning and development

Nice To Haves

Familiarity with regulatory intelligence platforms (e.g., Cortellis, Redica, Citeline, InfoDesk, FDA and EMA databases).

Responsibilities

Provide support to GxP Surveillance and GxP Intelligence Management System.
Actively and meticulously monitoring regulatory GxP requirements and expectations.
Daily screening and gathering new & changed regulations, guidance, trends, intelligence and regulatory enforcement activities with potential impact to BeOne products, processes and business in its priority markets.
Generation of daily reports for further assessment by the Triage Leads and subject matter experts from various GxP functions.
The regulatory surveillance on GxP (GLP, GCP, GVP, GMP, GDP/GSP, Pharmacopeia, Medical Device and Diagnostics, Drug-Device Combination product, Chemistry Manufacturing, Control (CMC), Supply Chain and Good AI Practice).
Efficient web searing and source evaluation.
Navigating regulatory authority websites (US FDA, EMA, PMDA, WHO, ICH, Pharmacopeia)
Monitoring updates, guidance documents, health authority notifications, alerts, and public consultation documents.
Document management – file organization and version control.