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?\n\nWe are recruiting for a start-up Medical Device company who are committed to improving patient outcomes through innovative medical technologies.\n\nWhat You'll Do:\n\nAs 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:\n\nLeading supplier management activities (SCARs, KPIs, audits, agreements)\nInvestigating complaints, non-conformances, and CAPAs\nInspecting and releasing products and labels\nReviewing Device History Records and equipment documentation\nSupporting internal and external audits\nDriving continuous improvement of the Quality Management System (QMS)\n\nWhat We're Looking For:\n\nEssential:\n\nExperience with ISO13485 and 21 CFR Part 820\nQA (and ideally QC) experience in a medical device company\nDegree or relevant quality qualificationDesirable:\n\n4+ years in a quality role within medical devices\nSupplier evaluation and monitoring expertise\nISO13485 Lead Auditor training\n\nKey Competencies:\n\n✅ High attention to detail\n✅ Strong collaboration and communication skills\n✅ Analytical and critical thinking\n✅ Ability to work independently and cross-functionally\n\nCarbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy