Global Regulatory Affairs Labeling Operations Intern

Company: Daiichi Sankyo
Location: Basking Ridge
Posted on: February 27, 2026

Job Description:

Job Description Job Title: Global Regulatory Affairs Labeling Operations Intern Job Requisition ID: 822 Posting Start Date: 2/24/26 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 Operations Intern for Summer 2026. This full-time position works 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 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) Additional Information 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. 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 Download Our Benefits Summary PDF Student

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