Lead the implementation activities for labeling under the responsibility of Global Labeling (GL) Operations, including:
Provision of Regulatory guidance on the development of U.S. packaging text for labeling mockups and production artwork
Request, review, and approve mockups and production artwork in the designated electronic artwork management system
Management of labeling implementation inputs and deliverables for registration sample packs, Software as a Medical Device (SaMD), and other non-U.S. labeling in scope of GL
Track implementation of artwork for safety changes and other types of labeling issued
Complete or provide input into Change Controls related to labeling implementation or delisting activities
Actively participate on project teams for launches, lifecycle changes, and Supply Chain-led labeling or packaging initiatives in partnership with Global Labeling Product Leaders, Supply Chain, Marketing, Regulatory Affairs, CMC Regulatory Affairs, Product Artwork, and others as needed
Provide timely and correct input and entries as needed in departmental labeling and project trackers
Update labeling history documents related to product artwork changes
Obtain and prepare labeling implementation input for U.S. Annual Reports
Assign National Drug Code (NDC) numbers and maintains NDC log for Johnson & Johnson Innovate Medicine and Patriot Pharmaceutical U.S.-marketed products
Support Establishment Registrations, Drug Listing, and Structured Product Labeling (SPL) for U.S.-marketed products
Support the Legal Department with litigation efforts related to GL-managed labeling, as needed
Provide feedback on U.S. Product Quality Complaints (PQC) related to product labeling and packaging artwork
Actively participate in or provide leadership of process improvement initiatives
Support audits and inspections, as needed
Requirements
A minimum of a Bachelor’s degree is required, preferably in a scientific discipline
A minimum of 4 years of relevant experience supporting labeling development, implementation, or operations is required
Experience in the Pharmaceutical industry is preferred
An understanding of pharmaceutical drug development is preferred
Knowledge of labeling processes and systems is required
Experience with NDA or BLA launches preferred
Understanding of audit and inspection processes and deliverables is preferred
Experience participating in continuous improvement projects is preferred
Experience in program/project management of quality and compliance activities associated with pharmaceutical labeling is preferred
Experience effectively/appropriately prioritizing and managing multiple projects simultaneously is preferred
Experience planning, scheduling, facilitating meetings across stakeholder groups is preferred
Experience working with dashboards and metrics (e.g., Tableau) preferred
Experience with Microsoft Office (Word, Excel, PowerPoint, Outlook), Teams tools and apps required
Must have excellent verbal and written communication skills
Must have strong organizational and negotiation skills
The ability to partner with cross-functional teams is required
The ability to drive a collaborative, customer-focused, learning culture is preferred
The ability to develop/deliver communications in a variety of settings for diverse audiences (e.g., announcements, newsletters, presentations) is preferred.