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Executive Director, Global Labeling

Bristol-Myers Squibb

Healthcare Jobs

Executive Director, Global Labeling

full-timePosted: Oct 28, 2025

Job Description

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, priority and plans: Identifies necessary resources in order to ensure that Global Labeling is adequately staffed and trained to fulfill its function in providing consistent standards of support and in achieving superior execution of plans. 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, as appropriate. Develops strong working relationships with the key stakeholders within Global Regulatory Sciences, within Drug Development, Medical, Global Product Development & Supply and BMS enterprise. Acts as a credible, influential and respected spokesperson and Is externally focused and results driven; 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. Oversee continuous improvement of E2E Labeling Initiative to establish well-documented optimized sustainable E2E labeling process with clear ownership, simplified process steps and increased compliance. Identifies trends in labeling-related regulatory authority compliance 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 with respect to labeling content and electronic labeling Keeps abreast of Regulatory changes, changes in authorities and requirements to enhance the effectiveness of the team and execution of regulatory deliverables Accountable for the effective and efficient execution of the E2E Labeling process as well as ensure full compliance with all internal and external regulatory requirements Ensures audit readiness and compliance with global regulatory standards and internal policies. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. 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.

Key Responsibilities

  • Build and lead a high-performing global labeling team
  • Foster a culture of excellence, accountability, and innovation
  • Recruit, develop, and retain top talent
  • Establish clear roles, responsibilities, and career development paths
  • Translate strategy into operational goals, priorities, and plans
  • Identify necessary resources to ensure Global Labeling is adequately staffed and trained
  • Influence internal and external stakeholders, including health authorities, to shape labeling outcomes
  • Define and establish effective processes, SOPs, and work practices
  • Develop strong working relationships with key stakeholders within Global Regulatory Sciences, Drug Development, Medical, Global Product Development & Supply, and BMS enterprise
  • Act as a credible, influential, and respected spokesperson
  • Optimize unit deliverables for speed to patient
  • Proactively manage Labeling Book of Work and monitor progress against submission timelines
  • Prioritize resources to meet company objectives
  • Oversee continuous improvement of E2E Labeling Initiative
  • Establish well-documented, optimized, sustainable E2E labeling process with clear ownership, simplified process steps, and increased compliance
  • Identify trends in labeling-related regulatory authority compliance enforcement, policies, and procedures
  • Incorporate trends into regulatory decisions and strategy
  • Provide strategic oversight of Labeling Management
  • Develop, review, and approve artwork for US, EU, and international packaging components
  • Ensure launch readiness for BMS products
  • Champion digital innovation, including e-labeling and structured content management
  • Participate and drive Global Labeling Policy, partnering with Global Regulatory Policy
  • Identify opportunities to influence regulatory policy and climate with respect to labeling content and electronic labeling
  • Keep abreast of regulatory changes, changes in authorities, and requirements
  • Enhance the effectiveness of the team and execution of regulatory deliverables
  • Ensure full compliance with all internal and external regulatory requirements
  • Ensure audit readiness and compliance with global regulatory standards and internal policies

Required Qualifications

  • PhD / Pharm D / MD or equivalent
  • 5 years of Pharma / R&D experience with broad regulatory experience
  • Thorough understanding of scientific principles, regulatory and business issues

Skills Required

  • Strategic vision and ability to set direction aligned with company objectives
  • Strong executive presence and influence across program teams and organizational initiatives
  • Ability to authentically build trusted relationships and collaborate across global, diverse, and multi-functional teams
  • Strong judge of talent with the ability to make tough talent decisions
  • Excellent communication and stakeholder engagement skills across functions and geographies
  • Experience in upskilling teams, promoting digital transformation, and embedding agile practices
  • Ability to assimilate and present complex scientific and regulatory information concisely
  • Understanding of regulatory implications of product strategy related to labeling development, assessment, and management
  • Strong problem-solving, decision-making, and analytical skills
  • Commitment to professional and ethical business practices
  • Digital-first mindset and ability to build digital capabilities across teams

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Locations

  • Princeton LVL, NJ
  • Madison, GIRALDA FARMS
  • Uxbridge, United States
  • Summit West, NJ

Salary

Estimated Salary Rangemedium confidence

200,000 - 300,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strategic vision and ability to set direction aligned with company objectivesintermediate
  • Strong executive presence and influence across program teams and organizational initiativesintermediate
  • Ability to authentically build trusted relationships and collaborate across global, diverse, and multi-functional teamsintermediate
  • Strong judge of talent with the ability to make tough talent decisionsintermediate
  • Excellent communication and stakeholder engagement skills across functions and geographiesintermediate
  • Experience in upskilling teams, promoting digital transformation, and embedding agile practicesintermediate
  • Ability to assimilate and present complex scientific and regulatory information conciselyintermediate
  • Understanding of regulatory implications of product strategy related to labeling development, assessment, and managementintermediate
  • Strong problem-solving, decision-making, and analytical skillsintermediate
  • Commitment to professional and ethical business practicesintermediate
  • Digital-first mindset and ability to build digital capabilities across teamsintermediate

Required Qualifications

  • PhD / Pharm D / MD or equivalent (experience)
  • 5 years of Pharma / R&D experience with broad regulatory experience (experience)
  • Thorough understanding of scientific principles, regulatory and business issues (experience)

Responsibilities

  • Build and lead a high-performing global labeling team
  • Foster a culture of excellence, accountability, and innovation
  • Recruit, develop, and retain top talent
  • Establish clear roles, responsibilities, and career development paths
  • Translate strategy into operational goals, priorities, and plans
  • Identify necessary resources to ensure Global Labeling is adequately staffed and trained
  • Influence internal and external stakeholders, including health authorities, to shape labeling outcomes
  • Define and establish effective processes, SOPs, and work practices
  • Develop strong working relationships with key stakeholders within Global Regulatory Sciences, Drug Development, Medical, Global Product Development & Supply, and BMS enterprise
  • Act as a credible, influential, and respected spokesperson
  • Optimize unit deliverables for speed to patient
  • Proactively manage Labeling Book of Work and monitor progress against submission timelines
  • Prioritize resources to meet company objectives
  • Oversee continuous improvement of E2E Labeling Initiative
  • Establish well-documented, optimized, sustainable E2E labeling process with clear ownership, simplified process steps, and increased compliance
  • Identify trends in labeling-related regulatory authority compliance enforcement, policies, and procedures
  • Incorporate trends into regulatory decisions and strategy
  • Provide strategic oversight of Labeling Management
  • Develop, review, and approve artwork for US, EU, and international packaging components
  • Ensure launch readiness for BMS products
  • Champion digital innovation, including e-labeling and structured content management
  • Participate and drive Global Labeling Policy, partnering with Global Regulatory Policy
  • Identify opportunities to influence regulatory policy and climate with respect to labeling content and electronic labeling
  • Keep abreast of regulatory changes, changes in authorities, and requirements
  • Enhance the effectiveness of the team and execution of regulatory deliverables
  • Ensure full compliance with all internal and external regulatory requirements
  • Ensure audit readiness and compliance with global regulatory standards and internal policies

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

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Bristol-Myers Squibb logo

Executive Director, Global Labeling

Bristol-Myers Squibb

Healthcare Jobs

Executive Director, Global Labeling

full-timePosted: Oct 28, 2025

Job Description

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, priority and plans: Identifies necessary resources in order to ensure that Global Labeling is adequately staffed and trained to fulfill its function in providing consistent standards of support and in achieving superior execution of plans. 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, as appropriate. Develops strong working relationships with the key stakeholders within Global Regulatory Sciences, within Drug Development, Medical, Global Product Development & Supply and BMS enterprise. Acts as a credible, influential and respected spokesperson and Is externally focused and results driven; 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. Oversee continuous improvement of E2E Labeling Initiative to establish well-documented optimized sustainable E2E labeling process with clear ownership, simplified process steps and increased compliance. Identifies trends in labeling-related regulatory authority compliance 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 with respect to labeling content and electronic labeling Keeps abreast of Regulatory changes, changes in authorities and requirements to enhance the effectiveness of the team and execution of regulatory deliverables Accountable for the effective and efficient execution of the E2E Labeling process as well as ensure full compliance with all internal and external regulatory requirements Ensures audit readiness and compliance with global regulatory standards and internal policies. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. 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.

Key Responsibilities

  • Build and lead a high-performing global labeling team
  • Foster a culture of excellence, accountability, and innovation
  • Recruit, develop, and retain top talent
  • Establish clear roles, responsibilities, and career development paths
  • Translate strategy into operational goals, priorities, and plans
  • Identify necessary resources to ensure Global Labeling is adequately staffed and trained
  • Influence internal and external stakeholders, including health authorities, to shape labeling outcomes
  • Define and establish effective processes, SOPs, and work practices
  • Develop strong working relationships with key stakeholders within Global Regulatory Sciences, Drug Development, Medical, Global Product Development & Supply, and BMS enterprise
  • Act as a credible, influential, and respected spokesperson
  • Optimize unit deliverables for speed to patient
  • Proactively manage Labeling Book of Work and monitor progress against submission timelines
  • Prioritize resources to meet company objectives
  • Oversee continuous improvement of E2E Labeling Initiative
  • Establish well-documented, optimized, sustainable E2E labeling process with clear ownership, simplified process steps, and increased compliance
  • Identify trends in labeling-related regulatory authority compliance enforcement, policies, and procedures
  • Incorporate trends into regulatory decisions and strategy
  • Provide strategic oversight of Labeling Management
  • Develop, review, and approve artwork for US, EU, and international packaging components
  • Ensure launch readiness for BMS products
  • Champion digital innovation, including e-labeling and structured content management
  • Participate and drive Global Labeling Policy, partnering with Global Regulatory Policy
  • Identify opportunities to influence regulatory policy and climate with respect to labeling content and electronic labeling
  • Keep abreast of regulatory changes, changes in authorities, and requirements
  • Enhance the effectiveness of the team and execution of regulatory deliverables
  • Ensure full compliance with all internal and external regulatory requirements
  • Ensure audit readiness and compliance with global regulatory standards and internal policies

Required Qualifications

  • PhD / Pharm D / MD or equivalent
  • 5 years of Pharma / R&D experience with broad regulatory experience
  • Thorough understanding of scientific principles, regulatory and business issues

Skills Required

  • Strategic vision and ability to set direction aligned with company objectives
  • Strong executive presence and influence across program teams and organizational initiatives
  • Ability to authentically build trusted relationships and collaborate across global, diverse, and multi-functional teams
  • Strong judge of talent with the ability to make tough talent decisions
  • Excellent communication and stakeholder engagement skills across functions and geographies
  • Experience in upskilling teams, promoting digital transformation, and embedding agile practices
  • Ability to assimilate and present complex scientific and regulatory information concisely
  • Understanding of regulatory implications of product strategy related to labeling development, assessment, and management
  • Strong problem-solving, decision-making, and analytical skills
  • Commitment to professional and ethical business practices
  • Digital-first mindset and ability to build digital capabilities across teams

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Locations

  • Princeton LVL, NJ
  • Madison, GIRALDA FARMS
  • Uxbridge, United States
  • Summit West, NJ

Salary

Estimated Salary Rangemedium confidence

200,000 - 300,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strategic vision and ability to set direction aligned with company objectivesintermediate
  • Strong executive presence and influence across program teams and organizational initiativesintermediate
  • Ability to authentically build trusted relationships and collaborate across global, diverse, and multi-functional teamsintermediate
  • Strong judge of talent with the ability to make tough talent decisionsintermediate
  • Excellent communication and stakeholder engagement skills across functions and geographiesintermediate
  • Experience in upskilling teams, promoting digital transformation, and embedding agile practicesintermediate
  • Ability to assimilate and present complex scientific and regulatory information conciselyintermediate
  • Understanding of regulatory implications of product strategy related to labeling development, assessment, and managementintermediate
  • Strong problem-solving, decision-making, and analytical skillsintermediate
  • Commitment to professional and ethical business practicesintermediate
  • Digital-first mindset and ability to build digital capabilities across teamsintermediate

Required Qualifications

  • PhD / Pharm D / MD or equivalent (experience)
  • 5 years of Pharma / R&D experience with broad regulatory experience (experience)
  • Thorough understanding of scientific principles, regulatory and business issues (experience)

Responsibilities

  • Build and lead a high-performing global labeling team
  • Foster a culture of excellence, accountability, and innovation
  • Recruit, develop, and retain top talent
  • Establish clear roles, responsibilities, and career development paths
  • Translate strategy into operational goals, priorities, and plans
  • Identify necessary resources to ensure Global Labeling is adequately staffed and trained
  • Influence internal and external stakeholders, including health authorities, to shape labeling outcomes
  • Define and establish effective processes, SOPs, and work practices
  • Develop strong working relationships with key stakeholders within Global Regulatory Sciences, Drug Development, Medical, Global Product Development & Supply, and BMS enterprise
  • Act as a credible, influential, and respected spokesperson
  • Optimize unit deliverables for speed to patient
  • Proactively manage Labeling Book of Work and monitor progress against submission timelines
  • Prioritize resources to meet company objectives
  • Oversee continuous improvement of E2E Labeling Initiative
  • Establish well-documented, optimized, sustainable E2E labeling process with clear ownership, simplified process steps, and increased compliance
  • Identify trends in labeling-related regulatory authority compliance enforcement, policies, and procedures
  • Incorporate trends into regulatory decisions and strategy
  • Provide strategic oversight of Labeling Management
  • Develop, review, and approve artwork for US, EU, and international packaging components
  • Ensure launch readiness for BMS products
  • Champion digital innovation, including e-labeling and structured content management
  • Participate and drive Global Labeling Policy, partnering with Global Regulatory Policy
  • Identify opportunities to influence regulatory policy and climate with respect to labeling content and electronic labeling
  • Keep abreast of regulatory changes, changes in authorities, and requirements
  • Enhance the effectiveness of the team and execution of regulatory deliverables
  • Ensure full compliance with all internal and external regulatory requirements
  • Ensure audit readiness and compliance with global regulatory standards and internal policies

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

Target Your Resume for "Executive Director, Global Labeling" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Executive Director, Global Labeling. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Executive Director, Global Labeling" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Answer 10 quick questions to check your fit for Executive Director, Global Labeling @ Bristol-Myers Squibb.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.