Global Regulatory Intelligence Lead

J&J Family of Companies; Leeds; Hybrid; GBP 70,000 - 90,000; Full time

Benefits offered by this job

Hybrid work options (Leeds, UK)

Job summary

Johnson & Johnson’s DePuy Synthes unit is seeking a Manager, Regulatory Intelligence to lead global monitoring of regulatory changes, guidance, and enforcement trends across health authorities. You will translate external signals into actionable insights to inform regulatory strategy and risk management across the product lifecycle.

The role requires collaboration with Regulatory Affairs, Quality, Medical Safety, and business partners, plus the ability to present leadership-ready reports.

Qualifications

• Typically 6–8 years of progressive experience in Quality, Regulatory Affairs, or Standards Compliance within a regulated industry (medical devices strongly preferred).
• Demonstrated experience interpreting and applying international standards and regulatory requirements.
• Strong understanding of quality management systems and compliance frameworks.

Responsibilities

• Lead end-to-end global monitoring of regulatory changes, guidance, and enforcement trends across key health authorities.
• Prepare clear, leadership-ready intelligence reports and risk summaries.
• Collaborate with Regulatory Affairs, Quality, Medical Safety, and business partners to translate intelligence into actionable plans.

Skills

Regulatory intelligence

Cross-functional collaboration

Data analytics

Risk assessment

Audits & inspections

Education

Bachelor's degree in Engineering/Life Sciences/Quality/Regulatory Affairs

Master's degree preferred

Tools

Regulatory databases

Analytics dashboards

Job description

Johnson & Johnson’s DePuy Synthes unit is seeking a Manager, Regulatory Intelligence to lead global monitoring of regulatory changes, guidance, and enforcement trends across health authorities. You will translate external signals into actionable insights to inform regulatory strategy and risk management across the product lifecycle.

The role requires collaboration with Regulatory Affairs, Quality, Medical Safety, and business partners, plus the ability to present leadership-ready reports.