Post Market Surveillance Supv

📋 Description

• Supervisory role within Regulatory Post Market Surveillance team
• Oversee complaint backlog, ensure productivity and accuracy
• Write/review file MDRs and Vigilance Reports
• Prepare responses to Regulatory agency requests
• Represent Regulatory Compliance at cross-functional meetings
• Perform classification/evaluation of complaints and escalate as needed

🎯 Requirements

• Undergraduate degree in engineering, life science, or equivalent
• 7+ years in medical device field
• Supervisory/lead experience in Medical Device company
• Strong knowledge of MDR/reporting requirements (US/EU)
• Mentor, communicate cross-functionally, strong organizational skills
• Ability to lead meetings, manage workload, attention to detail