Analyst Reg Aff in Leeds

Analyst Reg Aff in Leeds

Leeds Full-Time On-site
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At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world 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 MedTech, 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 jnj.com .

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Job Function

Regulatory Affairs Group

Job Sub Function

Regulatory Affairs

Job Category

Professional

All Job Posting Locations

Leeds, West Yorkshire, United Kingdom

DePuy Synthes is recruiting for a Analyst Reg Aff, located in Leeds, United Kingdom.

Content Compliance Specialist, EMEA (DePuy Synthes)

The Content Compliance Specialist plays a critical role in supporting the review and approval of advertising, promotional materials, and claims across the DePuy Synthes EMEA region. Acting as a moderator within the copy approval process, this role coordinates submissions, facilitates review activities, ensures compliance with established procedures, and supports timely delivery of compliant content to the business. The successful candidate will work closely with Marketing, Regulatory Affairs, Quality, and other cross-functional stakeholders to drive operational excellence, maintain audit-ready documentation, and continuously improve the efficiency and quality of content approval processes.

Key Responsibilities

  • Coordinate and moderate copy approval workflows for advertising, promotional materials, and claims.
  • Conduct submission quality and completeness reviews to ensure efficient processing.
  • Assign reviewers, facilitate review meetings, document outcomes, and track required follow-up actions.
  • Monitor submissions throughout approval, renewal, reapproval, and closure activities.
  • Provide process guidance and workflow support to submitters, reviewers, and stakeholders.
  • Maintain complete, accurate, and audit-ready records in accordance with applicable procedures and quality requirements.
  • Support SOP implementation, audit activities, CAPAs, and other quality and compliance initiatives.
  • Contribute to operational reporting and identify opportunities to improve submission quality, cycle times, and process efficiency.
  • Partner effectively with colleagues and stakeholders across multiple EMEA markets.

Qualifications

  • Bachelor's degree or equivalent professional experience.
  • Minimum 2 years of experience in Compliance, Quality, Regulatory Affairs, Content Review, Marketing Operations, or another regulated environment.
  • Experience working with approval workflows, documentation controls, and compliance processes.
  • Strong organizational skills with the ability to manage multiple priorities and deadlines.
  • Excellent communication and stakeholder management skills.
  • Fluent English required; additional European languages are an advantage.

What You'll Bring

  • Strong coordination and workflow management capabilities.
  • High attention to detail and commitment to quality.
  • Effective communication and stakeholder engagement skills.
  • Sound judgment and problem-solving abilities.
  • A continuous improvement mindset focused on delivering efficient and compliant business processes.

Join a dynamic regional team that enables compliant commercialization across DePuy Synthes EMEA. You'll have the opportunity to collaborate with diverse stakeholders, contribute to strategic business objectives, and help shape best-in-class content compliance operations in a highly regulated environment.

Support compliant and efficient content approval across DePuy Synthes EMEA by coordinating review workflows, partnering with stakeholders, and driving excellence in content compliance operations.

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject

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Analyst Reg Aff in Leeds employer: Johnson & Johnson Co.

At Johnson & Johnson, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work environment in High Wycombe, where innovation meets compassion. Our commitment to employee growth is evident through robust development opportunities and a culture that values diversity and collaboration, empowering you to make a meaningful impact in healthcare. Join us in our mission to transform lives while enjoying the benefits of a supportive workplace that champions your professional journey.

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Contact Details:

Johnson & Johnson Co. Recruitment Team