Quality Systems Engineer

I’m working on a fantastic Quality Systems Engineer opportunity with a fast-growing medical device business that’s recently completed an acquisition.

This role will be key in integrating the newly acquired company’s QMS into the existing quality framework. Once integration is complete, the focus will shift to maintaining and continuously improving the system, with a strong emphasis on compliance to global standards like ISO 13485:2016, MDR 2017/745, UK MDR 2002, and 21 CFR 820.

What you’ll be doing:

• Leading QMS integration and alignment projects
  
  
• Collaborating with cross-functional teams to identify and close gaps
  
  
• Supporting transition to a new eQMS platform
  
  
• Managing SOPs, forms, and documentation for ongoing compliance
  
  
• Handling CAPAs, NCRs, internal audits, supplier controls & QMS improvements
  
  
• Driving continuous improvement and lean quality initiatives
  
  
• Preparing for and supporting supplier and external audits
  
  What we’re looking for:
  
  
• Experience in a regulated/medical device environment
  
  
• Strong knowledge of ISO 13485, ISO 14971, MDR, 21 CFR Part 820
  
  
• Hands-on QMS integration/project experience
  
  
• Solid auditing, supplier management, and root cause analysis skills
  
  
• Excellent attention to detail, communication, and multitasking skills
  
  This is a great opportunity for someone who enjoys project ownership, cross-functional collaboration, and making a real impact in a scaling medtech business. If you’d like to hear more or know someone who’d be a good fit, feel free to drop me a message or apply to this advert with you updated CV