Key Responsibilities:
* Create and maintain labeling documents for medical devices in compliance with international regulatory standards.
* Collaborate with cross-functional teams including Regulatory, Quality, R&D, and Marketing.
* Ensure labeling documentation meets global standards and regional market needs.
Required Skills and Qualifications:
* Techical degree or certificate in a related field (e.g. technical writer, engineer).
* Relevant professional experience in labeling, quality, regulatory affairs or R&D, ideally in the medical device or pharmaceutical industries.
* Project management skills and ability to lead complex projects from creation to release.
About This Role:
This is a 12-month fixed-term contract position. The successful candidate will be responsible for creating and maintaining labeling documents for medical devices. They will work closely with internal and external stakeholders to ensure compliance with regulatory requirements. If you have a passion for labeling and technical publications, this role may be the perfect fit for you.