Quality Compliance Specialist
A company is looking for a Senior Specialist, Quality Compliance. Key Responsibilities Assess and investigate complaint information, escalating as necessary Prepare and submit Medical Device Reporting (MDR) reports to FDA Lead complaint investigations and manage customer relationships throughout the resolution process Required Qualifications Bachelor's Degree in a related field 5 years of experience in complaint handling Experience in a medical device or healthcare environment Proficient knowledge of Medical Device Reporting regulations Understanding of Good Documentation Practices (GDP) related to complaint filing
