Quality Compliance Specialist

Quality Compliance Specialist – Join a Team That Makes a Real Impact

Do you thrive on Quality, standards, audits, and the challenge of keeping products compliant in a fast‑moving global landscape? If you’re energised by solving problems, spotting gaps, and helping teams deliver their best, this is an opportunity to play a pivotal role at the heart of our Quality organisation.

• Monitoring new and evolving regulations and standards, assessing their impact on our products and Quality Management System
• Ensuring ongoing compliance by reviewing regulatory updates and aligning product claims, documentation, and processes
• Supporting compliance across the full product lifecycle — from early design and development through manufacturing and post‑market surveillance
• Identifying gaps in regulatory and standards compliance, coordinating cross‑functional actions, and driving timely closure
• Tracking and trending key quality and compliance activities, providing clear visibility of risks and progress to leadership
• Working with major global regulatory frameworks including EU MDR, ISO 13485, FDA 21 CFR Part 820/QMSR, Japan MHLW Ordinance 169, and other international requirements

You’ll be at the centre of global compliance, helping ensure our medical devices are safe, effective, and ready for markets worldwide. Your work will directly influence continuous improvement, strengthen our Quality System, and support teams across the organisation.

• Your contribution genuinely makes a difference to patients and products
• You’ll collaborate with a wide range of teams, technologies, and markets
• You’ll be part of a dynamic Quality function where compliance, improvement, and innovation come together

If you’re passionate about Quality and excited by the idea of shaping world‑class compliance, we’d love to welcome you to the team.