Intelerad seeks a Regulatory Affairs & Quality Specialist to maintain ISO 13485, MDSAP and CE mark, integrating regulatory requirements into process improvements. The role partners with the Regulatory Affairs & Quality Manager to enhance the management system and provide training.
The ideal candidate has 3+ years in quality management, strong regulatory knowledge, and experience in IT/medical devices, with a focus on audits, CAPAs, and cross‑functional collaboration.
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Contact Details:
Intelerad Medical Systems Incorporated Recruitment Team
