Product Labeling Specialist

12 months Fixed term contract Position Summary : Reporting to the Manager of the Label Development Team within the T&E Division. Responsible for supporting UDI compliant Label Development business initiatives for growth and sustaining product launches. Interface-cross functionally with teams internally and externally to align objectives and timelines. Support standardizations activities to improve global labeling objectives across department functions, this includes device identification, label data, equipment requirements and configuration management to improve global labeling operations in compliance with our organizations global quality policy and company values. What you will do : Create, revise, and manage product Labels (Main focus on Labels and label templates) in compliance with regulatory requirements. Collaborate with cross-functional teams including Regulatory, Quality, R&D, and Marketing. Ensure labeling documentation meets global standards and regional market needs. Support product development and lifecycle management projects with accurate technical publications. Assist with audits, regulatory submissions, and change control processes. What you will need? You have successfully completed a technical degree or gained a certificate in a related field (e.g. technical writer, engineer). You have many years of relevant professional experience in labeling, quality, regulatory affairs or R&D, ideally in the medical device, pharmaceutical or other regulated industries. You have experience in project management and are highly efficient in leading the process from creation to release. You have a keen interest in the implementation of projects as well as the creation and maintenance of high-quality documents. You are fluent in spoken and written English and ideally have knowledge of German and / or French. You are a resilient, reliable and service-oriented person who enjoys working on complex issues in a qualitative and timely manner. You feel comfortable in an international work environment and can integrate easily into various (project) teams. Tools : Prisym 1.6 / Labeling Software tools / Quality Management Systems / Medical Device #IJ This role will be posted for a minimum of 3 days. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login / Register.