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An exciting opportunity has arisen for an experienced Label Strategy Manager (Devices) to join a European labelling team on a maternity cover basis. This role will take end‑to‑end responsibility for European device and drug‑product labelling, ensuring compliance, consistency and strategic alignment across the product lifecycle.
Job Responsibility
Develop, maintain and implement EU device and drug-product labelling in line with EU MDR, SmPC and internal quality standards
Lead European device labelling strategy and represent labelling at cross-functional Labelling Strategy and Operations forums
Ensure alignment and consistency of key messages across labelling documents, artwork and patient information
Review, author and quality-check labelling documents to meet submission and implementation timelines
Collaborate closely with Regulatory Affairs, Operations, Supply Chain, affiliates and global partners across regions
Requirements
5-7 years' experience in Regulatory Affairs, R&D or a related discipline, with strong exposure to EU device and/or drug-product labelling
Solid working knowledge of EU MDR and European labelling regulations for medical devices and pharmaceuticals
Proven ability to manage complex projects, timelines and multiple stakeholders in a regulated environment
Strong communication, influencing and problem-solving skills, with a collaborative team mindset
Bachelor's degree in Pharmacy, Life Sciences or a related field