Job Description

Overview Join to apply for the Executive Director Global Labeling role at Bristol Myers Squibb . The Executive Director, Global Labeling is a senior leadership position responsible for shaping and executing global regulatory labeling strategies to support company objectives and patient needs. This role leads a high-performing team of Labeling Strategists, ensuring timely, efficient, and compliant development and maintenance of labeling documents for US, EU, and international markets. The Executive Director has oversight for these key capabilities: Global Labeling Strategy : oversee the development and implementation of regulatory labeling strategies to meet BMS objectives and patient needs; manage a team of Labeling Strategists who ensure timely, efficient, and compliant labeling development and maintenance. Global Labeling Management : provides labeling and regulatory operational support to US, EU and International Markets. Global Labeling Compliance : executive oversight to ensure compliance with regulations, timeliness of delivery, and quality of labeling content. Global Process Owner for End-to-End Labeling Processes : provide decisions and oversight to Process Leads, drive process optimization, sustain and drive continuous improvement, and define/process metrics to achieve Quality Outcomes. Global Labeling Policy : drives and influences key labeling policy topics and participates in external industry forums. Head of Cross-functional Labeling Office : oversees the end-to-end labeling process from label development through delivery of labeling to end users in packaging/digital labeling. Key responsibilities Builds and leads a high-performing global labeling team, fostering excellence, accountability, and innovation. Recruits, develops, and retains top talent with the right mix of skills and experience. Establishes clear roles, responsibilities, and career development paths to support team growth and engagement. Translates strategy into operational goals, priorities, and plans; ensures Global Labeling is adequately staffed and trained to provide consistent standards of support and superior execution. Influences internal and external stakeholders, including health authorities, to shape labeling outcomes. Defines and establishes effective processes, SOPs, and work practices to drive consistency and efficiency. Develops strong working relationships with key stakeholders within Global Regulatory Sciences, Drug Development, Medical, Global Product Development & Supply, and the BMS enterprise. Acts as a credible, influential spokesperson with an externally focused, results-driven orientation; optimizes unit deliverables for speed to patient. Proactively manages Labeling Book of Work and monitors progress against submission timelines; prioritizes resources to meet Company objectives. Oversees continuous improvement of the End-to-End Labeling initiative to establish a well-documented, optimized, sustainable process with clear ownership, simplified steps, and increased compliance. Identifies trends in labeling-related regulatory authority enforcement, policies and procedures; incorporates into regulatory decisions and strategy. Strategic oversight of Labeling Management responsible for development, review, and approval of artwork for US, EU and international packaging components and ensure launch readiness for BMS products. Champions digital innovation, including e-labeling and structured content management. Participates and drives Global Labeling Policy, partnering with Global Regulatory Policy; identifies opportunities to influence regulatory policy and climate regarding labeling content and electronic labeling. Keeps abreast of regulatory changes and requirements to enhance team effectiveness and execution of regulatory deliverables. Accountable for the effective and efficient execution of the End-to-End Labeling process and for full compliance with internal and external regulatory requirements. Ensures audit readiness and compliance with global regulatory standards and internal policies. Requirements PhD / PharmD / MD or equivalent, with thorough understanding of scientific principles, regulatory and business issues, and 15 years of Pharma / R&D experience with broad regulatory expertise. Demonstrates strategic vision and the ability to set direction aligned with company objectives. Exhibits strong executive presence and influence across program teams and organizational initiatives. Authentically builds trusted relationships and collaborates across global, diverse, and multi-functional teams to drive business objectives. Serves as a strong judge of talent with the ability to make tough talent decisions. Possesses excellent communication and stakeholder engagement skills across functions and geographies. Has experience in upskilling teams, promoting digital transformation, and embedding agile practices. Assimilates and presents complex scientific and regulatory information concisely. Understands regulatory implications of product strategy related to labeling development, assessment, and management. Demonstrates strong problem-solving, decision-making, and analytical skills. Commits to professional and ethical business practices. Fosters a digital-first mindset and builds digital capabilities across teams. Note: The Executive Director, Global Labeling is a senior leadership position responsible for shaping and executing global regulatory labeling strategies to support company objectives and patient needs. This role leads a high-performing team of Labeling Strategists, ensuring timely, efficient, and compliant development and maintenance of labeling documents for US, EU, and international markets. The Executive Director has oversight for these key capabilities as listed above. Seniority level Executive Employment type Full-time Job function Business Development, Product Management, and Quality Assurance Industries Pharmaceutical Manufacturing #J-18808-Ljbffr Bristol Myers Squibb

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