3/13更新的Regulatory Affairs Summer Intern---暑期實習

工作內容

• 需求人數

  ：1人
• Position Summary You will join the Regulatory Affairs team in Taiwan as a summer intern. You will support regulatory activities that help bring safe and effective healthcare solutions to patients. You will work with people across regulatory, medical, quality, and commercial teams. We value clear communication, attention to detail, curiosity, and teamwork. This role offers practical learning, meaningful impact, and exposure to regulatory processes that support GSK’s mission of uniting science, technology and talent to get ahead of disease together. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Help prepare and maintain regulatory submission dossiers and supporting documents for local regulatory authority review. - Assist in compiling and organising regulatory correspondence, meeting minutes, and submission trackers. - Support review and cross-checking of label, package insert, and promotional materials for regulatory adherence. - Collect, collate and summarise technical and administrative information from internal teams to support regulatory filings. - Monitor local regulatory updates and guidance; prepare short summaries to inform the team. - Contribute to administrative tasks that support regulatory processes, including filing, version control and audit-ready documentation. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals - Currently enrolled in a bachelor’s or master’s degree in life sciences, pharmacy, regulatory affairs, public health, or a related field. - Strong written and spoken Mandarin; good English communication skills. - Able to work on-site in Taiwan; this role is primarily on-site during the summer period and may offer limited hybrid working during the academic term depending on team needs. - Comfortable with routine document work and following standard operating procedures. - Proficient in Microsoft Office applications (Word, Excel, PowerPoint). - Able to work well in a team, meet deadlines, and manage multiple tasks. Preferred Qualification If you have the following characteristics, it would be a plus - Previous internship or project experience in regulatory affairs, quality, clinical operations, or related areas. - Basic understanding of regulatory submission formats and common regulatory documents (for example, summaries, templates, or dossiers). - Experience using document management systems or version control tools. - Familiarity with local regulatory authority processes in Taiwan. - Attention to detail with experience in editing or proofreading technical documents. - Interest in patient safety, product lifecycle, and a career in regulatory affairs. What you will learn and gain - Practical exposure to regulatory submission preparation and document management. - Cross-functional collaboration experience with regulatory, medical, quality, and commercial teams. - Mentoring and structured feedback to develop regulatory skills and professional habits. - A clearer view of career paths in regulatory affairs and related functions. Intern Duration : One Year intern -From 2026/July /01 - 2027/June /31 -Summer : Full time ( July / August ) - School time : maxium 20 hours per week Term PT : TWD 210/ Hour Full Time : TWD 33,600 / Month