A company is looking for a Quality Manager to oversee compliance with quality management systems in a medical device environment.
Key Responsibilities : Implement and maintain quality systems in compliance with cGMP and ISO13485 standardsLead investigations and manage deviations, change controls, CAPAs, and complaintsConduct internal audits and manage product quality reviews to ensure regulatory complianceRequired Qualifications : Bachelor's degree in a technical field (e.
g., Biology, Chemistry, Engineering)5+ years of experience in quality management within a manufacturing environmentKnowledge of quality control methodologies and tools (e.
g., Six Sigma, Lean)Familiarity with regulatory requirements and standards (e.g., ISO, AAMI, FDA, cGMP)
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