<Back to Search
Manager, Global Labeling - Remote
RemoteMarch 26th, 2026
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.Job Summary Reporting to the Director of Global Labeling, the Manager, Global Labeling is responsible for supporting Global Labeling Leads in daily operational labeling activities (US and global); managing and maintaining US SPL, drug listings, and establishment registrations; triaging, reviewing, and tracking Country Product Information (CPI); and performing operational activities that support Global Labeling deliverables and responsibilities. The primary responsibilities will bestructured product labelingandmaintaining drug listings .Essential FunctionsCollaborate with key stakeholders to facilitate and lead cross-functional teams in the development, review, approval, and maintenance of the establishment registration and drug listing (bulk and finished) in the US.Perform bi-annual review and submission of FDA-required drug listings and establishment registrations.Act as a Subject Matter Expert (SME) on US Structured Product Labeling (SPL): Provide guidance and support for the U.S. drug listings and Structured Product Labeling (SPL), partner with an external service provider to deliver on SPL commitments.Collaborate with global stakeholders and stay abreast of structured product labeling developments, requirements, and formats in rest of world.Be familiar with National Drug Code (NDC), Dun and Bradstreet Number (DUNS), FDA Establishment Identification (FEI), and Global Trade Identification Number (GTIN) requirements.Review and track requests for updates to Country Product Information (CPI) and CPI components. This includes QC, proofing, copy editing and formatting of documents, and coordinate review by Global Labeling Lead.Attend necessary labeling team meetings to discuss decisions regarding any label and CPI updates, discuss any findings of meaningful differences among Source Reference Labels (SRLs) and CPIs.Represent the Global Regulatory Services and Operations (GRSO), Global Labeling Group on project teams.Support the use and development of current and new tools, technologies, and processes to support global label development, submission, approval, and dispatch of Source Reference Labels in and to respective countries in addition to global label support.Track periodic CCDS reviews to ensure compliance with internal procedures and timelines.Maintain labeling history documents and assist in responding to labeling-related queries from various functional areas.Ensure all actions taken within role follow applicable SOPs and associated documents so that high quality delivery of outputs and compliance is maintained.Ensure appropriate tracking of labeling projects via defined procedures and optimal use of systems.Participate in and contribute to the continuous improvement efforts related to business practices and tools utilized within role.Contribute and support the development and maintenance of job aids and guidance documents.Support compliance activities including audits, inspections, and labeling-related escalations and non-conformances.RequirementsBS degree (or higher) in life scienceA minimum of 4 years of experience in the pharmaceutical industry is requiredA minimum of 2 years of experience in product labeling/labeling regulations is requiredCan demonstrate strong project management, problem solving, strategic thinking, negotiation, interpersonal and communication skills (both written and oral), attention to detail and ability to work under tight timelines, and across teams and regionsPossess experience in both local and global regulatory labeling environments and work on multiple projectsMust be a team-oriented individual with personal commitment to human relations, integrity, giving and receiving feedback, adaptability, and a diverse working environmentAble to work under pressure and enforce company-wide standardsMust possess a strong working knowledge of Microsoft Office applications, document management systems, labeling text verification systems as well as related labeling software and trackersThe annual base salary range for the Manager, Global Labeling - Remote is from :$100,000-$131,300Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan. Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.Certain other benefits may be available for this position, please discuss any questions with your recruiter.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.E-Verify ParticipationRight To WorkE-Verify Participation#J-18808-Ljbffr
Showing 400 of 65,645 matching similar jobs in Springbrook, ND
- Senior Product Manager
- Senior Consultant - Regulatory Operations Software Implementation (Remote)
- Physician / Non Clinical Physician Jobs / Delaware / Permanent / Physician Compensation Analyst
- Managed Services Consultant - Quality (Remote)
- Physician / Radiology / Florida / Permanent / Radiology Physician
- Physician / Non Clinical Physician Jobs / Delaware / Permanent / Senior Physician, Patient Safety (S
- Physician / Non Clinical Physician Jobs / New Hampshire / Permanent / Physician Compensation Analyst
- Physician / Administration / Iowa / Permanent / Physician Compensation Analyst
- Physician / Non Clinical Physician Jobs / Massachusetts / Permanent / Senior Physician, Patient SafeSuffolk, VAMarch 28th, 2026
- Physician / Non Clinical Physician Jobs / Utah / Permanent / Senior Physician, Patient Safety (Senio
- Physician / Non Clinical Physician Jobs / New Hampshire / Permanent / Senior Physician, Patient Safe
- Physician / Non Clinical Physician Jobs / Puerto Rico / Permanent / Physician Compensation Analyst
- Salesforce Project Coordinator
- Salesforce Project Coordinator
- US Medical Affairs Lead, Oncology - Prostate/GI
- Clinical Project, Feasibility Analytics Manager
- Salesforce Project Coordinator
- Sr. Manager, Regulatory Affairs
- Regulatory Affairs Associate
- Salesforce Project Coordinator
- Regulatory Affairs Specialist II
- Regulatory Affairs Associate
- Senior Manager, Clinical Operations
- Senior Product Manager - Clinical Attrition Risk & Engagement
- Physician / Gastroenterology / South Carolina / Permanent / Gastroenterology Physician Job near Columbia, SC Job
- Physician / Gastroenterology / South Carolina / Permanent / Gastroenterology Physician Job near Columbia, SC
- CMC Regulatory Dossier Management Director
- Global Offshore Revenue Supervisor, VA (REMOTE)
- Physician / Orthopedics / Kentucky / Permanent / BC/BE Orthopedic Surgeon Needed Near Shelbyville, KY Job
- Physician / Urgent Care / Oregon / Permanent / Full-Time Urgent Care Physician - Beautiful Southern Oregon - High Comp Job
- Staff Global Program Manager
- Coding Compliance Analyst
- Program/Project Manager
- Regional Total Rewards Sr Analyst (APAC & EMEA)
- CRA II - Midwest
- Project Manager I - Cell & Gene Therapy (Sponsor-Dedicated/ Hybrid- LosAngeles))
- Product Manager - Global Studio
- Licensing Consultant - North America Client Licensing team
- Program Coordinator, Regional APC Lead
- Contract Compliance Specialist