Manager, Label Strategist (Regulatory Affairs)

Label Strategy Manager (Devices) – Europe

Location: Maidenhead/Remote (Hybrid working model)Contract: Temporary, full-time (7‑month maternity cover), starting July 2026Rate: Negotiable – circa. £60-70 per hour

Overview

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.

Key Responsibilities

• 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

Skills & Experience Required

• 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 (advanced degree desirable)

To Apply: Please contact Theo Charles.

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