Analyst Reg Aff (Content Compliance Specialist, EMEA)

Johnson & Johnson’s orthopaedics business, DePuy Synthes, is recruiting a Regulatory Affairs Analyst (Content Compliance Specialist, EMEA) in Cape Town, with hybrid working. You will moderate the copy approval process for advertising, promotional materials and claims across the EMEA region, coordinating reviews and keeping records audit-ready. (The same role is also advertised in Leeds, UK, under a separate requisition.)

Key responsibilities:

Coordinate and moderate copy approval workflows for advertising, promotional materials and claims
Check submissions for quality and completeness so they move through quickly
Assign reviewers, run review meetings, record outcomes and follow up on actions
Track submissions through approval, renewal, reapproval and closure
Guide submitters, reviewers and stakeholders on the process
Keep complete, accurate, audit-ready records and support SOPs, audits and CAPAs
Contribute to reporting and improve submission quality and cycle times across EMEA markets
Requirements:

Bachelor’s degree or equivalent professional experience
At least 2 years in compliance, quality, regulatory affairs, content review, marketing operations or another regulated environment
Experience with approval workflows, document control and compliance processes
Strong organisation, communication and stakeholder management skills
Fluent English; other European languages are an advantage
Posted: 22 October 2026. Closing date: 29 October 2026. Requisition R-106571. J&J plans to separate its orthopaedics business into a standalone company (DePuy Synthes), and the successful candidate would be expected to move with it.