A family-owned IVD manufacturer with over 60 years of history and 70 employees is seeking a QA/RA Manager to take full ownership of Quality and Regulatory Affairs. The company has strong financial backing, its own distribution and regulatory function, and is part of the Norway National Association.Responsibilities:Lead and develop a small QA/RA team of threeMaintain and manage ISO 13485 QMSOversee regulatory strategy and new product registrationsEnsure ongoing compliance across the full product lifecycleWork cross-functionally across R&D, manufacturing, and operationsAct as the strategic owner of QA/RA activities within the businessRequirements:510 years experience in QA/RA within IVD or medical devicesPrevious leadership responsibility (small team ideal)Strong experience with ISO 13485 and regulatory submissionsAble to operate strategically while remaining hands-onExperience in a small company or cross-functional environment preferredScandinavian language skills essential Why Join? 60-year company with strong backing and long-term vision High ownership role with real strategic impact Hybrid working 4 days onsite in Billingstad (flexible when needed)If you are interested apply below or reach out on: lcattcamfield@barringtonjames.com +44 (0) 1293 776644