Global Regulatory Affairs Labeling Operations Intern - Remote Eligible

Global Regulatory Affairs Labeling Operations Intern

Join a Legacy of Innovation 125 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 18,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group's 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.

We are currently seeking a Global Regulatory Affairs Labeling Operations Intern for Summer 2026. This full-time position works approximately 37.5 hours per week.

Position Summary: We are seeking a detail-oriented and tech-savvy student to join our Global Regulatory Affairs Labeling Operations team as an intern. The Global Regulatory Affairs Labeling function strategically develops high-quality, differentiated labeling defining the distinct characteristics of our products. Within GRAL, Labeling Operations designs processes and implements digital and technology tools to enable efficiency and compliance, including automation and generative AI. This role will have an opportunity to work on business initiatives with an emphasis on process improvement, technology entablements, and other projects to gain experience with compliance-related labeling activities. The candidate will gain hands-on experience managing team projects and interacting with senior leaders. The ideal candidate will be comfortable working with software applications and possess a strong interest in operational efficiency and the use of technology to enable processes within a regulated environment.

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 as needed, such as tracking and reporting activities.
• Participate in team discussions and provide input on operational best practices.
• Schedule routine meetings with the necessary stakeholders, prepare meeting materials and minutes, and follow up on action items.
• Develop an approach and a project plan to address assigned project.
• Maintain metrics and tracking of progress on project.
• Development and delivery of 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 (e.g., Microsoft Office Suite). Experience with other technology platforms such as 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.
• Candidates must be a self-starter with capability to develop creative solutions.
• Candidates must be available to work full-time for 12 weeks (June through August).

Preferred Skills:

• Interest in regulatory labeling operations and process optimization.
• Experience with project coordination or operational support in a corporate setting.
• Familiarity with compliance concepts in a pharmaceutical or life sciences environment.

Salary Range: $17.23 - $58.15

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. All 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.