Changing lives. Building Careers. Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what's possible and making headway to help improve outcomes. We are seeking a detail-oriented **Quality Assurance Inspector** to join our team and ensure the accuracy and compliance of medical devices and components processed in a **GMP-rated, FDA, and MOD-regulated environment** . The ideal candidate thrives in a meticulous role, possesses excellent organizational skills, and understands the critical importance of inspection, testing, and data integrity in medical device manufacturing. You will play a vital role in upholding quality standards, maintaining compliance, and supporting operational efficiency. In this role, you will: + Perform inspections and tests of finished devices, sub-assemblies, and components using appropriate inspection, measurement, and test (IMT) equipment. + Review and interpret engineering drawings, material specifications, and test documents (training in technical drawing interpretation will be provided). + Support **incoming inspection** processes using various metrology equipment to ensure compliance with specifications. + Collaborate with supply chain and manufacturing teams to plan inspection activities and ensure priorities are achieved. + Manage non-conforming materials and communicate issues to management promptly. + Analyze trends in failures or anomalies, implement immediate corrective actions, and ensure follow-up measures are executed. + Maintain accurate, compliant documentation and records in accordance with **cGMP** and medical device regulations. + Perform additional tasks as directed by the **QA Manager** . **Essential Requirements** + Minimum **2 years** of experience in an **FDA** and **ISO 13485** regulated manufacturing facility. + Previous experience in a quality inspection role, preferably in a **medical device manufacturing** environment. + Strong attention to detail, data accuracy, and document control. + Ability to effectively communicate with management, peers, and cross-functional teams. **Preferred Skills** + Familiarity with metrology tools, IMT equipment, and technical drawing interpretation. + Experience conducting **failure trend analysis** and implementing corrective actions. + Knowledge of **cGMP** and FDA/ISO standards. **Soft Skills** + Strong planning, organizational, and time-management abilities. + Effective interpersonal communication and the ability to work both collaboratively and independently.