A company is looking for a Global Labeling Lead Specialist to manage labeling projects for medical device products.
Key Responsibilities
Lead labeling artwork development and revisions, assessing regulatory impacts on product labels
Coordinate with cross-functional teams to verify labeling content and resolve feedback conflicts
Support health authority submissions and monitor project timelines for labeling changes
Required Qualifications
Bachelor's degree or higher preferred; 8 years of relevant industry experience may substitute
Knowledge of medical device industry and regulatory affairs throughout the product lifecycle
Proficiency in Adobe Acrobat and Microsoft Office programs
Experience with product labeling processes and regulatory approvals
Strong analytical reasoning and critical thinking abilities
Labeling Specialist • Newark, Delaware, United States