Global Serialization Intern

Posted 22 Days Ago
Be an Early Applicant
Raleigh, NC, USA
In-Office
25-25 Hourly
Internship
Healthtech • Pharmaceutical • Manufacturing
The Role
The Global Serialization Intern will support day-to-day operations of the serialization system, assist with documentation and process improvement, and participate in cross-functional collaboration for supply chain compliance.
Summary Generated by Built In

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference.  If this is your profile, we want to hear from you.

Eisai is seeking an intern to join our team for a 6-month assignment. You will have the opportunity to support team members by assisting with day-to-day operational tasks, documentation, and system support related to Eisai’s Global Serialization Enterprise System (rfXcel) and related platforms. You will also actively participate in connectivity projects and process improvement initiatives, helping to ensure the enterprise system remains efficient and resilient. Additionally, this role involves contributing to Business Continuity and Crisis Management efforts, building organizational resilience, and mitigating risk. Designed as a structured learning opportunity, the position offers hands-on experience with pharmaceutical serialization, GS1 standards, and global supply chain compliance while providing meaningful operational support.
Working under the guidance of Global Serialization Business Analysts, Technical Analyst, and the Project Manager, you will contribute to SOP maintenance, master data activities, issue triage, and cross-functional coordination. You will gain exposure to system upgrades and connectivity projects and will play a supporting role in process improvement and Business Continuity and Crisis Management activities across the serialization function.

Essential Functions

• Support Global Serialization team members in the day-to-day operation of the Global Serialization Enterprise System (rfXcel).
• Assist with documentation updates, including SOPs, work instructions, and training materials related to serialization processes.
• Support master data maintenance activities across serialization, government, and third-party systems.

• Assist with the creation of simulated test files to facilitate system testing and validation activities.

• Participate in basic incident triage and troubleshooting activities, escalating issues appropriately to senior team members.
• Support ongoing process improvement initiatives and documentation harmonization efforts across the Global Serialization organization.
• Observe and support integration qualification activities and informal testing activities as part of system lifecycle management.
• Participate in global team meetings and cross-functional collaboration to build understanding of serialization operations and compliance requirements.

Requirements

  • At least 18 years of age prior to scheduled start date

  • Hybrid role requiring onsite presence Tuesday through Thursday

  • Must be currently enrolled in a Bachelors degree program in Supply Chain, Information Technology, Engineering, Business, or a related field.

  • Interest in pharmaceutical supply chain, serialization, or regulatory compliance.

  • Strong proficiency with Microsoft O365 applications (Excel, Word, PowerPoint, Teams, CoPilot, OneNote, Outlook).

  • Ability to learn new enterprise systems and technical concepts quickly.

  • Ability to thoughtfully apply emerging technologies, including AI tools, to improve efficiency, accuracy, and workflow effectiveness under guidance.

  • Awareness of responsible AI use, including data privacy, confidentiality, and appropriate application within enterprise systems.

  • Ability to work together with other members of a project team to accomplish objectives.

  • Critical thinker and problem solver with excellent communication skills

Eisai Salary Transparency Language:

The hourly rate for the Global Serialization Intern is : $25.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status.  Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

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The Company
Nutley, NJ
2,984 Employees
Year Founded: 1985

What We Do

At Eisai Inc., human health care (hhc) is our goal. We give our first thought to patients and their families, and helping to increase the benefits health care provides. As the U.S. pharmaceutical subsidiary of Tokyo-based Eisai Co., Ltd., we have a passionate commitment to patient care that is the driving force behind our efforts to discover and develop innovative therapies to help address unmet medical needs. Eisai is a fully integrated pharmaceutical business that operates in two global business groups: oncology and neurology (dementia-related diseases and neurodegenerative diseases). Each group functions as an end-to-end global business with discovery, development, and marketing capabilities. Our U.S. headquarters, commercial and clinical development organizations are located in New Jersey; our discovery labs are in Massachusetts and Pennsylvania; and our global demand chain organization resides in Maryland and North Carolina. To learn more about Eisai Inc., please visit us at www.eisai.com/US. Comments and posts by users on this site are not created or controlled by Eisai Inc. and Eisai is not responsible for such content

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