Job Opportunity:
Product Labeling Specialist
This position is responsible for creating and maintaining labeling documents for high-quality medical devices. As the first point of contact for internal and external customers, you will ensure that labeling documentation meets global standards and regional market needs.
Key Responsibilities:
* Create, revise, and manage product labels and label templates
* Collaborate with cross-functional teams including Regulatory, Quality, R&D, and Marketing
* Develop and implement labeling processes to meet regulatory requirements
* Support product development and lifecycle management projects with accurate technical publications
* Assist with audits, regulatory submissions, and change control processes
Requirements:
* Technical degree or certificate in a related field (e.g., technical writer, engineer)
* Many years of relevant professional experience in labeling, quality, regulatory affairs, or R&D, ideally in the medical device, pharmaceutical, or other regulated industries
* Experience in project management and efficient process leadership
* Fluency in spoken and written English and knowledge of German and/or French desirable
* Resilient, reliable, and service-oriented individual with a keen interest in project implementation and high-quality document creation