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 and drives the end‑to‑end labeling operations for US, EU, and international markets.
Working with Us
Challenging. Meaningful. Life‑changing. You will work on groundbreaking projects from optimizing production lines to the latest breakthroughs in cell therapy, transforming the lives of patients and the careers of our team.
Key Responsibilities
* Builds and leads a high‑performing global labeling team, fostering a culture of excellence, accountability, and innovation.
* Recruits, develops, and retains top talent, ensuring the team has 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 and identifies necessary resources to ensure that Global Labeling is adequately staffed and trained to fulfill its function and deliver consistent standards of 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 and respected spokesperson, externally focused and results driven, optimizing unit deliverables for speed to patient.
* Proactively manages Labeling Book of Work and monitors progress against submission timelines, prioritizing resources to meet company objectives.
* Oversees continuous improvement of the end‑to‑end labeling initiative to establish a well‑documented, optimized, sustainable labeling process with clear ownership, simplified process steps and increased compliance.
* Identifies trends in labeling‑related regulatory authority compliance enforcement, policies and procedures; incorporates them into regulatory decisions and strategy.
* Strategically oversees labeling management responsible for development, review and approval of artwork for US, EU and international packaging components and ensures 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 to identify opportunities to influence regulatory policy and climate with respect to labeling content and electronic labeling.
* Keeps abreast of regulatory changes, authorities and requirements to enhance the effectiveness of the team and execution of regulatory deliverables.
* Accountable for the effective and efficient execution of the end‑to‑end labeling process and ensures full compliance with all internal and external regulatory requirements.
* Ensures audit readiness and compliance with global regulatory standards and internal policies.
Requirements
* PhD / Pharm D / MD or equivalent, with thorough understanding of scientific principles, regulatory and business issues with 15 years of pharma / R&D experience with broad regulatory experience.
* 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.
Compensation Overview
$259,530 - $314,490
The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. Eligibility for specific benefits listed on our careers site may vary based on the job and location.
Benefits
Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals—both at work and in their personal lives—including medical, pharmacy, dental, vision, 401(k), paid vacation, parental leave, wellness programs, and more.
Equal Employment Opportunity
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. For more information visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
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