Regulatory Affairs - Summer Intern

Business Introduction
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
Find out more:
Our approach to R&D


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.

Why You?

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.

Internship details

• Duration: One year intern program with summer full-time period; typical dates July 1, 2026 to August 31, 2026.
• Location: Taiwan; primarily on-site with potential for limited hybrid working during term-time.

How to apply
We would love to hear from you. Please submit your CV and a short note (200 words max) explaining why this role excites you and what you hope to learn. If you have relevant coursework, project reports, or work samples, feel free to include them. Apply now and help us unite science, technology and talent to get ahead of disease together.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact APACRecruitment.Adjustments@gsk.com. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.

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