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Exp Anlst Reg Aff

Job in Churwell, LS27, England, UK
Listing for: 7355-Johnson & Johnson Medical Limited Legal Entity
Full Time position
Listed on 2026-10-18
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 70000 - 90000 GBP Yearly GBP 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Location: Churwell

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, and solutions are personal.

Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at  As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Regulatory Affairs Group

Job Sub Function:

Regulatory Affairs

Job Category:

Professional

All Job Posting Locations:

Leeds, West Yorkshire, United Kingdom

Job Description:

DePuy Synthes is recruiting for a Exp Anlst Reg Aff, located in Leeds, United Kingdom. Lead Content Compliance Specialist, EMEA (DePuy Synthes)

About the Role

The Lead Content Compliance Specialist is a key regional expert responsible for coordinating and optimizing advertising, promotional material, and claims approval processes across DePuy Synthes EMEA. The role partners with cross-functional stakeholders to ensure compliant, efficient, and business-focused execution of copy approval activities while driving operational excellence, quality oversight, and continuous improvement. This position serves as a trusted advisor to the business, providing operational leadership, managing complex and high-priority submissions, identifying risks, and driving process enhancements that improve customer experience, scalability, and business continuity.

Key Responsibilities
  • Lead and coordinate regional copy approval operations across the EMEA region.
  • Provide subject matter expertise and operational guidance for complex, multi-market, and business-critical submissions.
  • Monitor service, compliance, quality, and cycle-time performance and drive data-based improvements.
  • Identify and mitigate operational, compliance, and process risks.
  • Support audit readiness, SOP implementation, quality processes, and procedural compliance.
  • Develop performance insights and recommendations for leadership decision-making.
  • Lead implementation of process, system, and operational changes to improve effectiveness and scalability.
  • Build strong partnerships with Marketing, Regulatory Affairs, Quality, and other cross-functional stakeholders.
  • Support the evolution of future operating models, governance frameworks, and service-provider capabilities.
Qualifications
  • Bachelor's degree or equivalent experience.
  • 4-5+ years of experience in Compliance, Regulatory Affairs, Quality, Content Governance, or related functions.
  • Experience working in regulated environments with complex cross‑functional processes.
  • Demonstrated ability to manage stakeholders, resolve operational challenges, and drive continuous improvement.
  • Strong analytical, communication, and problem‑solving skills.
  • Fluent in English; additional European languages are an advantage.
What You'll Bring
  • Expertise in compliance and governance processes.
  • Strong operational leadership and decision‑making skills.
  • Ability to influence and collaborate across a complex matrix organization.
  • Experience using data and insights to improve performance and drive change.
  • Passion for delivering compliant, efficient, and customer‑focused solutions.
Required Skills

Analytical Reasoning, Business Behavior, Business Writing, Communication, Confidentiality, Data Reporting, Detail-Oriented, Legal Support, Medicines and Device Development and Regulation,…

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