Labeling Associate, I
Core
Support the Regulatory Documentation Team in developing and approving product labeling for medical and pharmaceutical products, ensuring compliance with medical, legal, and regulatory requirements.
Role type
Labeling Specialist (Regulatory Affairs)
Builds
Product labeling artwork and documentation for medical/pharmaceutical products
Domain
Medical devices and pharmaceuticals
Deliverable
product features
Required skills
Project prioritization, stakeholder collaboration, regulatory compliance evaluation, lifecycle implementation strategy, issue resolution, financial impact analysis
Preferred skills
Supply chain experience, quality assurance background, regulatory affairs background
Responsibilities
Prioritize and drive labeling projects to completion; Gather and evaluate information for labeling changes; Facilitate cross-functional reviews of product labeling; Coordinate resolution of labeling development issues; Ensure adherence to standards and work instructions; Advise management on potential exposure risks.