Product Labeling Specialist
In this role, you will be responsible for the creation and maintenance of labeling documents for high-quality medical devices in accordance with international regulatory standards.
* Create, revise, and manage product labels in compliance with regulatory requirements.
* Collaborate with cross-functional teams to ensure labeling documentation meets global standards and regional market needs.
* Support product development and lifecycle management projects with accurate technical publications.
You will work in a world-class and quality-focused environment ensuring timely delivery of proper information to customers. You will be required to have a strong understanding of regulatory affairs, project management skills, and the ability to work in a complex and dynamic environment.
Required Skills and Qualifications:
* Technical degree or certificate in a related field (e.g., technical writing, engineering).
* Relevant professional experience in labeling, quality, regulatory affairs, or R&D, ideally in the medical device, pharmaceutical, or other regulated industries.
* Project management skills and experience leading processes from creation to release.
* Excellent communication and teamwork skills.
* Fluency in spoken and written English and ideally knowledge of German and/or French.
As a Product Labeling Specialist, you will be responsible for creating and maintaining accurate and compliant labeling documents that meet regulatory requirements. If you are a detail-oriented individual with excellent project management skills and a passion for working in a fast-paced environment, we encourage you to apply for this exciting opportunity.