Global Regulatory Affairs Labeling Intern

Daiichi Sankyo, Inc.; Basking Ridge (NJ); On-site; USD 24,000 - 80,000; Full time

Job summary

Daiichi Sankyo, Inc. invites students to join its Global Regulatory Affairs Labeling team for Summer 2027.

The internship runs about 37.5 hours per week for 12 weeks, providing hands-on experience in labeling operations, cross-functional collaboration, and project documentation. As an intern, you will support process improvements, help track milestones, prepare materials for meetings, and develop reports on project outcomes while gaining exposure to regulatory labeling concepts in a leading

Qualifications

• Currently enrolled in a graduate or undergraduate program.
• Proficiency with Microsoft Office; Veeva Vault and SharePoint a plus.
• Familiarity with automation, AI, and technology tools.
• Strong written and verbal communication.
• Able to work independently in a fast-paced environment.
• Availability for 12 weeks full-time (June–August).

Responsibilities

• Support labeling operations projects to improve processes.
• Identify workflow enhancements and support implementations.
• Collaborate with cross-functional teams to track labeling initiatives.
• Prepare materials for meetings and project documentation.
• Contribute to compliance-related tracking and reporting.
• Create project plans and maintain progress metrics.
• Develop presentations and reports on outcomes.
• Schedule meetings and document minutes.

Skills

Attention to detail

Organizational skills

Written and verbal communication

Independent work

Self-starter

Creative problem solving

Time management

Education

Graduate or undergraduate program in Regulatory Affairs or related field

Tools

Microsoft Office

Veeva Vault

SharePoint

Job description

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Job Summary

We are currently seeking a Global Regulatory Affairs Labeling Intern for Summer 2027. This position works for approximately 37.5 hours per week.

Responsibilities

• Support labeling operations projects focused on improving processes and operational efficiency.
• Assist in identifying opportunities for workflow enhancements and contribute to implementation efforts.
• Collaborate with cross-functional teams to gather input and track progress on labeling initiatives.
• Prepare materials for team meetings, presentations, and project documentation.
• Contribute to compliance-related tasks such as tracking and reporting activities.
• Participate in team discussions and provide input on operational best practices.
• Schedule routine meetings with stakeholders, prepare meeting materials and minutes, and follow up on action items.
• Develop an approach and project plan to address assigned projects.
• Maintain metrics and track progress on projects.
• Develop and deliver presentations and reports on project outcomes.

Qualifications

• Currently enrolled in a graduate or undergraduate program (e.g., Regulatory Affairs, PharmD, Scientific, Public Health, Information Technology or related field).
• Proficiency with software applications such as Microsoft Office Suite; experience with Veeva Vault and SharePoint is a plus.
• Proficiency with automation, generative AI, and other technology tools.
• Excellent attention to detail and organizational skills.
• Strong written and verbal communication abilities.
• Ability to work independently and manage multiple tasks in a fast-paced environment.
• Prior experience in a regulated industry or with process improvement projects is a plus but not required.
• Self-starter with capability to develop creative solutions.
• Availability to work full-time for 12 weeks (June through August).
• Interest in regulatory labeling operations and process optimization preferred.
• Experience with project coordination or operational support in a corporate setting preferred.
• Familiarity with compliance concepts in a pharmaceutical or life sciences environment preferred.

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range

USD$17.23 - USD$58.15