Labeling Lead

Johnson & Johnson Innovative Medicine • Cincinnati, OH

1d • $94,000 - $151,800

About The Position

Johnson & Johnson MedTech, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Lebeling Lead, located in Cincinnati, Ohio. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/ (https://www.jnj.com/). ABOUT MEDTECH Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness.
We are seeking a detail-oriented and strategic Labeling Lead to be responsible for the development and management of product labels for both New Product Development (NPD) and Lifecycle Management (LM) projects. This key role leads all aspects of the end-to-end execution of labeling changes, ensuring alignment with artwork, label components, and regulatory compliance. The ideal candidate will support business objectives by driving label content updates that reflect regulatory requirements, supply chain strategies, and company standards, ultimately ensuring accurate and compliant labeling across all product lines.

Requirements

• Bachelors Degree required
• 6-8 Years of Relevant Work Experience
• A solid track record of effective project management, ensuring timely delivery of labeling activities.
• Demonstrated ability to run multiple projects simultaneously, maintaining quality and adherence to deadlines.
• Proven understanding of Medical Device or equivalent regulated industry, Quality Systems and Change Control procedures.
• Demonstrated ability to lead a cross-functional cross region team.

Responsibilities

• Lead collaboration efforts to capture requirements and alignment on label strategy and content with cross-functional teams including Regulatory, Clinical, Quality, R&D, and Product Lifecycle Management, as needed.
• Manage labeling execution planning by coordinating with project teams to align label development activities with project timelines, escalating and resolving capacity constraints through prioritization, capacity augmentation, or adjusting project timelines in collaboration with stakeholders.
• Lead all aspects of the execution of Design Control documentation and ensure compliance with established procedures for label development.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level