Senior Manager, Global Labeling

Eisai$129K — $169K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • BS degree or higher in life science
  • 8+ years of experience in drug development
  • 3-5 years of regulatory experience in the pharmaceutical industry
  • Experience with global and/or local regulatory labeling environments preferred
  • In-depth knowledge of FDA and EU labeling guidelines, with familiarity in Asia
  • Strong project management and people management skills

Responsibilities

  • Lead cross-functional teams for CCDS and CPI development
  • Provide regulatory guidance for global labeling content and design
  • Manage a team of direct reports
  • Ensure US CPI regulations compliance through accurate labeling
  • Maintain labeling history and respond to inquiries regarding labeling
  • Stay updated on global labeling guidelines and regulations
  • Contribute to special projects within GRN or GL structures

Benefits

  • Participation in the annual incentive plan
  • Access to comprehensive company benefits programs
  • Opportunities for professional development and training
  • Flexible work arrangements
  • Collaborative work environment fostering cross-functional initiatives
Full Job Description
The Senior Manager, Global Labeling facilitates and leads the development, review, approval, and maintenance of the Company Core Data Sheets (CCDS) for assigned products and the Country Product Information (CPI) and CPI components for assigned products either globally as a Global Labeling Lead or regional/local as a Regional Labeling Lead. The Senior Manager, Global Labeling represents the Global Regulatory Network (GRN) Global Labeling Group on project teams and acts as a Subject Matter Expert (SME) on local, regional and multi-country regulatory labeling requirements and participate in the sharing of intelligence. The Senior Manager, Global Labeling follows Global Labeling procedures and maintains relevant databases and document management systems for assigned products. Essential Functions • Coordinate and lead cross-functional teams in the development and lifetime maintenance of the TPP, CCDS and Country Product Information (CPI) and CPI components for assigned products/projects. This includes QC, proofing, copy editing and formatting of documents, and coordinate review and approval of final submission. 30% • Provide tactical and strategic guidance to CPI development teams regarding regulatory requirements, content and design for TPP, CCDS, CPI and CPI components for assigned products on a global basis. 25% • Manage direct reports. 10% • Coordinate Content of Labeling/Drug Listing SPL generation and review to ensure compliance with US CPI regulations. 10% • Maintain labeling history documents and assist in responding to labeling-related queries from various functional areas. Maintain expertise regarding key labeling requirements worldwide and stay current with labeling guidelines and regulations on a global basis. 15% • Participate or lead special assignments related to GRN, GL or other cross-functional processes and/or activities. 10% Requirements • Minimum BS degree or higher in life science. • 8+ years of experience in drug development environment, with minimum 3-5 years of regulatory experience within the pharmaceutical industry. • Experience in global and/or local regulatory labeling environments is preferred. • Demonstrate a solid working knowledge of drug development process, as well as FDA and EU labeling; knowledge of and experience with Asia and other markets labeling desirable. • Competent knowledge of and demonstrated ability to apply regulatory guidelines pertaining to product labeling and ICH guidelines. • Demonstrate strong project management, people management, problem solving, strategic thinking, negotiation, interpersonal and communication skills (both written and oral) attention to detail and ability to work under tight timelines. Eisai Salary Transparency Language: The annual base salary range for the Senior Manager, Global Labeling is from :$129,000-$169,300 Under 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.

About Eisai

Eisai Co., Ltd. is a Japanese pharmaceutical company headquartered in Tokyo, Japan. It has some 10,000 employees, among them about 1,500 in research. Eisai is listed on the Tokyo Stock Exchange and is a member of the Topix 100 and Nikkei 225 stock indices.
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