REGULATORY AFFAIRS INTERN

We have an exciting opportunity for you as a Regulatory Affairs Intern with our Client, a global pharmaceutical company, Novo Nordisk.

For over 100 years, Novo Nordisk has been driven by a purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger - a legacy of impact that reaches far beyond today.

Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job - you're becoming part of a story that spans generations

What We Offer

• Opportunity to learn and contribute to impactful projects.
• For Post-Grad, monthly internship stipend of $2,000
• For Under-Grad, monthly internship stipend of $1,600

As a Regulatory Affairs Intern, you will:

• Update key data points in planning excel sheets, including statuses on submissions and approvals, to support strategic planning and documentation of regulatory considerations.
• Ensure system updates and data compliance from key affiliates.
• Create and manage team communications such as quarterly digests, project newsletters, and sharing best practices from regulatory advocacy activities and workshops.
• Contribute to strategic projects such as APAC shared pack & e-labelling and support the pilot project for implementing KPIs related to system compliance.

Your skills & qualifications
We are looking for a motivated and enthusiastic individual who:

• Currently pursuing an undergraduate degree in Pharmacy, Medicine or Biology.
• Excellent written and verbal communication, with digital fluency, creativity
• Conscientious self-starter with good organizational skills, project management skills and attention to detail.
• Interpersonal communication and ability to collaborate with teams; must effectively operate independently, across functional lines, and with internal customers.
• Proficient in Microsoft Office Tools including Word, Excel, PowerPoint, etc.

Your new department
You will be part of the Regulatory Affairs team within the APAC Regulatory function. Based in the dynamic APAC region, our team is dedicated to ensuring compliance and driving strategic regulatory initiatives. We foster a collaborative and supportive atmosphere where curiosity and innovation are encouraged. Join us to contribute to impactful projects and gain valuable experience in a fast-paced and engaging environment.

Deadline
31 March 2026. Applications are reviewed on an ongoing basis, and the position may be closed before the deadline.

Interested applicants, please send in your resume to [Confidential Information]
LAU QUET ENG (R1110677)
MANPOWER STAFFING SERVICES (S) PTE LTD (02C3423)

Gwen, Quet Eng Lau EA License No.: 02C3423 Personnel Registration No.: R1110677

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