Director, Global Labeling

3 weeks ago


Cambridge, United States Eisai Full time

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. The Director, Global Labeling is responsible for the leadership and oversight of the Labeling function within Global Regulatory Services and Operations (GRSO). This position will manage labeling operations and actively contribute to the development and implementation of regulatory labeling strategy and documentation for marketed products and products in development. This job serves as an expert on regulations governing labeling of pharmaceutical products globally, and serves as the global regulatory labeling representative on relevant project teams to provide strategic input into the development and approval of Target Product Profile (TPP) for development products and all Eisai product Company Core Data Sheets (CCDSs), US Package Inserts (PIs), European Union (EU) Summary of Product Characteristics (SmPCs) and Emerging Market labels. This position manages a team of professionals located in the US and UK, and is responsible for employee-related activities, including resource management, performance management, coaching and mentoring on both operational and strategic aspects of labeling, and fostering a culture of proactive people development. Essential Functions Lead cross-functional teams in the timely development of content for a new or revised CCDS, USPI, EU SmPC and Emerging Markets labels for assigned products, following internal procedures for review, approval and implementation of labels. Acts as liaison between co-promote partners and Eisai stakeholders in the labeling process. Establish and maintain processes and standards for global labeling. Supervise direct reports to effectively operationalize labeling activities across all products. Develop and mentor direct reports on both operational and strategic aspects of labeling. Responsible maintaining the Drug and Establishment Listings for all of Eisai's products. Maintain centralized labeling repository within Eisai's electronic document management system for all global labels at various stages of development, review and approval. Manage labeling development, review and approval workflows within the electronic documents management system and track the timely and consistent implementation of safety changes in local labels. Provide labeling support for Eisai US and EU Packaging Engineering functions for artwork control and approval. Ensure consistency of labeling across product lines and compliance with Eisai policies and procedures and applicable regulatory authority directives and regulations. Analyze competitor labeling and ensure Eisai products have most competitive labeling. Manage a team of professionals in the US and UK. Responsible for all employee-related activities throughout the year, including performance management and development. Maintain expertise regarding key labeling requirements worldwide and stay current with labeling guidelines and regulations by FDA, EMA and other applicable regulatory authorities. Represent the Global Labeling group on Regulatory Sub‑Teams and other project teams to communicate key strategies. Requirements Bachelors degree in life sciences required; higher degree preferred Minimum of 10 years of experience in Regulatory, R&D or related area Pharmaceutical experience required Solid working knowledge of drug development process Solid working knowledge and experience of global regulatory labeling environments and requirements Solid knowledge of and demonstrated ability to apply regulatory guidelines pertaining to product labeling and ICH guidelines. Strong project management, people management, problem solving, strategic thinking, negotiation, interpersonal and communication skills (written and oral) Ability to work under tight timelines Attention to detail This position is remote based in Nutley, NJ (Tuesday, Wednesday, Thursday in office). We will consider the possibility of remote based. Eisai Salary Transparency Language The annual base salary range for the Director, Global Labeling is from :$180,700-$237,200. Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term 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. 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: Right To Work E-Verify Participation #J-18808-Ljbffr



  • Cambridge, United States Eisai Full time

    Director, Global LabelingAt Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care 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...


  • Cambridge, United States Eisai Inc. Full time

    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...


  • Cambridge, United States Eisai Full time

    A leading pharmaceutical company is seeking a Director, Global Labeling to oversee labeling operations and manage the regulatory strategy for products. This role involves leading cross-functional teams, ensuring compliance with regulations, and mentoring a team across the US and UK. Ideal candidates will have extensive experience in pharmaceutical labeling...


  • Cambridge, MA, United States Beam Therapeutics Inc. Full time

    Company Overview: Beam Therapeutics is a clinical stage biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform that includes a suite of gene editing and delivery technologies and is in the process of building internal manufacturing...


  • Cambridge, United States Moderna Full time

    The Role Within an end-to-end (E2E) labeling framework, manage a team of labeling strategy leads responsible for, in partnership with the GRS Strategy team, ensuring the development and implementation of regulatory labeling strategies to meet Moderna's company objectives and the needs of patients. This leader closely partners with the GRS Head of Labeling...


  • Cambridge, United States Moderna Full time

    The Role Within an end-to-end (E2E) labeling framework, manage a team of labeling strategy leads responsible for, in partnership with the GRS Strategy team, ensuring the development and implementation of regulatory labeling strategies to meet Moderna's company objectives and the needs of patients. This leader closely partners with the GRS Head of Labeling...


  • Cambridge, United States Akebia Full time

    Associate Director Regulatory LabelingRegulatory AffairsCambridge, MAID: 25R-26Full-Time/RegularNearly 37 million Americans are currently affected by Chronic Kidney Disease. 37 million. At Akebia we take that number very seriously and every day we come to work, with the purpose of bettering the lives of each person impacted by kidney disease and the renal...


  • Cambridge, United States Beam Therapeutics Full time

    Beam Therapeutics is a clinical stage biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform that includes a suite of gene editing and delivery technologies and is in the process of building internal manufacturing capabilities. Beam’s...


  • Cambridge, Massachusetts, United States Beam Therapeutics Full time $200,000 - $250,000 per year

    Company Overview:Beam Therapeutics is a clinical stage biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform that includes a suite of gene editing and delivery technologies and is in the process of building internal manufacturing...


  • Cambridge, MA, United States Akebia Therapeutics Full time

    Associate Director Regulatory LabelingLinkedIn Twitter Email Message ShareRegulatory Affairs Cambridge, MA * ID: 25R-26* Full-Time/RegularNearly 37 million Americans are currently affected by Chronic Kidney Disease. 37 million. At Akebia we take that number very seriously and every day we come to work, with the purpose of bettering the lives of each...