Regulatory and Pharmacovigillance Intern

Regulatory & Pharmacovigilance Intern
Clinical, Medical & Regulatory
Jakarta, Indonesia

Join Novo Nordisk Indonesia as a Regulatory Affairs (RA) & Pharmacovigilance (PV) Intern and support our team in preparing regulatory submissions, engaging with local health authorities, and monitoring medicine safety. You’ll gain exposure to global standards, patient access initiatives, and cross-functional collaboration in a dynamic and purpose-driven environment.

Your new role
The internship opportunity will give you the opportunity to develop skills sets that will be beneficial to your future career growth such as regulatory submission, ensuring safety and compliance of medicine. Our team is small, close-knit, agile, fun, and highly motivated, passionate about driving change for patients. As a Regulatory & Pharmacovigilance Intern you will:

• Prepare and submit regulatory affairs (RA) documents for BPOM and pharmacovigilance (PV).
• Ensure 100% compliance with timeline submissions for RA and PV.
• Provide administrative support for monitoring and reporting (M&R) projects.
• Internship duration: 5 January 2026 – 31 July 2026.
• Working hours Monday to Friday, 9am – 5pm (inclusive of lunch hour).
• Location: Jakarta, Indonesia.
• Internship allowance will be given.

Your new department
You will be joining the Clinical, Medical & Regulatory department at Novo Nordisk. This dynamic team is dedicated to ensuring regulatory compliance for new products and product amendments, safeguarding patient safety, and maintaining our license to operate. The Regulatory Affairs function focuses on gaining regulatory approval for clinical trials, new drugs, devices, and digital health solutions, while also shaping future regulatory frameworks through collaboration with health authorities and policymakers. The Safety Pharmacovigilance function ensures the safety of our medicines, collecting and analysing safety data, and addressing any product safety issues. 

Your skills & qualifications
To succeed in this role, we are looking for candidates with the following qualifications:

• Recent graduate from pharmacy.
• Strong in project management skills.
• An open-minded and collaborative mindset. 
• Interest or experience in regulatory affairs and pharmacovigilance. 
• Proficiency in Microsoft environment. You will be guided on internal systems throughout the internship. 

Working at Novo Nordisk 
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.
 
Deadline
24 November 2025. Applications are reviewed on an ongoing basis, and the position may be closed before the deadline.

Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.

Novo Nordisk is not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.

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