Medical Device Labeling Specialist
Job Summary
In this key role, you will be responsible for creating and maintaining labeling documents for medical devices in compliance with international regulatory standards.
You will serve as the primary point of contact for internal and external customers, collaborating with cross-functional teams to ensure accurate and timely delivery of labeling documentation.
Key Responsibilities
* Create, revise, and manage product labels in compliance with regulatory requirements.
* Collaborate with Regulatory, Quality, R&D, and Marketing teams to ensure global standards are met.
* Support product development and lifecycle management projects with accurate technical publications.
Requirements
To be successful in this role, you will need:
* A degree in a related field (e.g. technical writing, engineering) or equivalent experience.
* Multiple years of relevant professional experience in labeling, quality, regulatory affairs, or R&D.
* Excellent project management skills, with the ability to lead complex processes from creation to release.
Benefits
This is an exciting opportunity to join our team and contribute to the success of our organization.
We offer a dynamic work environment, opportunities for growth and development, and a competitive compensation package.
About Us
We are a leading provider of medical devices, committed to delivering high-quality products that meet the needs of our customers.