Are you passionate about quality and compliance in the medical device industry? Do you thrive in a dynamic environment where your attention to detail and problem-solving skills make a real impact?

We are recruiting for a start-up Medical Device company who are committed to improving patient outcomes through innovative medical technologies.

What You'll Do:

As a Quality Engineer, you'll play a key role in both Quality Assurance and Quality Control functions, ensuring product safety and regulatory compliance. Your responsibilities will include:

• Leading supplier management activities (SCARs, KPIs, audits, agreements)
• Investigating complaints, non-conformances, and CAPAs
• Inspecting and releasing products and labels
• Reviewing Device History Records and equipment documentation
• Supporting internal and external audits
• Driving continuous improvement of the Quality Management System (QMS)

What We're Looking For:

Essential:

• Experience with ISO13485 and 21 CFR Part 820
• QA (and ideally QC) experience in a medical device company
• Degree or relevant quality qualification

Desirable:

• 4+ years in a quality role within medical devices
• Supplier evaluation and monitoring expertise
• ISO13485 Lead Auditor training

Key Competencies:

✅ High attention to detail
✅ Strong collaboration and communication skills
✅ Analytical and critical thinking
✅ Ability to work independently and cross-functionally

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.