Manager, Global Labeling Product Leader
Johnson & Johnson
Posted: 10/20/2026
Senior Product Manager, Shared Hosting
Newfold Digital
Posted: 10/20/2026DNSLAMPSQLWordPress
Associate Product Owner
Sigma Systems
Posted: 10/20/2026CloudGoogle Cloud PlatformSDLC
Product Owner
Fusable
Posted: 10/20/2026
Staff Product Manager
Walmart
Posted: 10/20/2026
Product Manager
AlertMedia
Posted: 10/20/2026
Product Manager
Thermo Fisher Scientific
Posted: 10/20/2026
Data Product – AI Query Governance
Bank of America
Posted: 10/20/2026
Senior Product Manager, Agent Platform
CGWS - COME GROW WITH US
Posted: 10/20/2026
Consumer Compliance Lead – Product Advisory, Testing
Nubank
Posted: 10/20/2026
Principal AI Product Management
TransUnion
Posted: 10/20/2026Manager, Global Labeling Product Leader
Johnson & Johnson
Posted: 10/20/2026
Lead Digital Product Manager
Wells Fargo
Posted: 10/20/2026
Senior Product Manager, Epic Optimization
Ensemble Health Partners
Posted: 10/20/2026
Senior Manager, Product Management – Enterprise API Platforms, API Governance
Capital One
Posted: 10/20/2026Manager, Product Management – Enterprise API Gateway, API Runtime
Capital One
Posted: 10/20/2026Manager, Product Management – Enterprise API Platforms, API Design
Capital One
Posted: 10/20/2026
Staff Product Manager – AV Capabilities
General Motors
Posted: 10/20/2026
Staff Product Manager – Forward Deployment
BetterUp
Posted: 10/20/2026
Senior Product Manager – Streamlit
Snowflake
Posted: 10/20/2026CloudOpen SourcePython
Manager, Global Labeling Product Leader
Johnson & JohnsonCore Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in pharmaceutical labeling processes, including the development and maintenance of primary labeling documents and compliance with regulatory guidelines. Proven ability to lead project teams and contribute to continuous improvement initiatives within the pharmaceutical industry.
Highest-signal resume keywords
Pharmaceutical Drug DevelopmentRegulatory Affairs ExperienceLabeling RegulationsDocument Management SystemsProject Management
About the role
Key responsibilities & impact- Lead development, revision, review, agreement, and maintenance of primary labeling documents for assigned compounds
- Manage the Company Core Data Sheet, United States Package Insert, associated patient labeling, and European Union Product Information
- Manage derived labeling documents and labeling text for the EU and US
- Recommend and advise on labeling content, processes, timelines, and scientific integrity
- Coordinate resolution of labeling issues affecting primary or derived labeling and supporting documentation
- Ensure high-quality and compliant labeling documents
- Contribute to global labeling strategy, including competitor therapeutic-area analysis and development-plan assessment
- Apply knowledge of labeling aspects to development of labeling and target labeling
- Contribute to continuous improvement of the end-to-end labeling process
Requirements
What you’ll need- A minimum of Bachelor’s degree in a scientific discipline is required
- A minimum of 4 years of relevant experience in the pharmaceutical industry is required
- An understanding of pharmaceutical drug development is required
- Experience in discussing and communicating scientific concepts is required
- Basic understanding of worldwide regulatory guidelines and their applications for labeling is required
- Experience leading project teams within a matrix environment
- Ability to work largely independently with limited supervision
- Demonstrated proactive approach
- Experience participating in continuous improvement projects
- Exceptional verbal and written communication, organizational, negotiation and partnering skills
- Experience working in document management systems
- Advanced degree (MS, PhD, MD or PharmD) is preferred
- A minimum of 3 years of Regulatory Affairs experience with product labeling/labeling regulations, or equivalent, is preferred
- Successful track record of prioritizing and managing multiple products and projects simultaneously is preferred
- Demonstrated ability to drive a collaborative, customer-focused, learning culture is preferred
Benefits
Comp & perks- Consolidated retirement plan (pension)
- Savings plan (401(k))
- Vacation – 120 hours per calendar year
- Sick time – 40 hours per calendar year
- Holiday pay, including Floating Holidays – 13 days per calendar year
- Work, Personal and Family Time – up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period
- 10 days
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
- Inclusive interview process and accommodation support
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Labeling Document DevelopmentCore Data Sheet ManagementLabeling Content RecommendationCompetitor Therapeutic-Area AnalysisScientific Integrity Assessment
Soft Skills
Exceptional Communication SkillsOrganizational SkillsNegotiation SkillsProactive ApproachCollaborative Culture Development
Certifications & Qualifications
Bachelor’s Degree in Scientific DisciplineAdvanced Degree (MS, PhD, MD, PharmD)
Industry Keywords
Pharmaceutical IndustryRegulatory GuidelinesLabeling Process ImprovementMatrix Environment ExperienceContinuous Improvement Projects