
Content Creation Specialist
2 weeks ago
This role involves the creation, revision, and management of labeling documents for medical devices. The successful candidate will work in a world-class environment ensuring that proper information is delivered to customers to enable safe use of our devices.
- Create labels and technical documentation in compliance with regulatory requirements.
- Collaborate with cross-functional teams including Regulatory, Quality, R&D, and Marketing.
- Ensure labeling meets global standards and regional market needs.
- Support product development and lifecycle management projects.
The ideal candidate will have relevant professional experience in labeling, quality, or regulatory affairs, as well as project management skills and the ability to lead complex projects from creation to release.
This position offers an opportunity to work in an international environment and contribute to making healthcare better through innovative products and services.
Key Responsibilities:
- Product Labeling and Documentation: Create, revise, and manage product labels and technical documentation.
- Cross-Functional Collaboration: Collaborate with internal and external stakeholders.
- Regulatory Compliance: Ensure labeling meets global standards and regional market needs.
- Project Management: Lead complex projects from creation to release.
Requirements:
- Education: Technical degree or related field certificate.
- Experience: Relevant professional experience in labeling, quality, or regulatory affairs.
- Skills: Project management, leadership, and communication.
We offer: A challenging and dynamic work environment, opportunities for professional growth, and a chance to contribute to making healthcare better.
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