Manager, Label Strategist (Regulatory Affairs)

Carbon 60
Maidenhead, Berkshire, United Kingdom
6 months ago
£60 – £70 ph
Applications closed

Related Jobs

View all jobs
Spotlight

Senior Regulatory Affairs & Quality Manager

Bluetree Cambridge, Cambridgeshire, United Kingdom
£65,000 – £80,000 pa Hybrid

Manager, Medical Writing, Immunology

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site

Manager Clinical Data Transparency, Data Sharing

Johnson & Johnson MedTech High Wycombe, United Kingdom

Manager, Global Labeling Product Leader

Johnson & Johnson MedTech High Wycombe, United Kingdom

Manager, Quality Clinical Risk Management

Johnson & Johnson MedTech High Wycombe, United Kingdom

Manager Clinical Data Transparency, Data Sharing

Johnson & Johnson MedTech Netherlands

Manager Clinical Data Transparency, Data Sharing

Johnson & Johnson MedTech
Hybrid

Salary

£60 – £70 ph

Posted
16 Apr 2026 (6 months ago)

Label Strategy Manager (Devices) - Europe

Location: Maidenhead/Remote (Hybrid working model)

Contract: Temporary, full-time (7‑month maternity cover), starting July 2026

Rate: Negotiable - circa. £60-70 per hour

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 regionsSkills & 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 click below and/or to discuss further, contact Theo Charles on (phone number removed)

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.