Post Market Surveillance Supv

📋 Description

• Oversee Regulatory Post Market Surveillance team for productivity and accuracy
• Provide guidance and feedback to team; ensure completeness of complaint and Regulatory reporting
• Manage regulatory reporting including MDR and Vigilance to align with procedures
• Analyze quality data to support Regulatory Compliance activities

🎯 Requirements

• Education: undergraduate degree in engineering, life science, or equivalent
• Experience: 7+ years in medical device field; supervisory/lead experience in medical devices
• Knowledge of Medical Device Complaint files and regulatory reporting (US FDA, EU MDR)
• Skills: mentoring, cross-functional communication, strong organizational skills
• Leadership: ability to guide direct reports, conduct performance reviews, manage workloads
• Strong written/verbal communication and Excel/PowerPoint/database skills

🎁 Benefits

• On-site weekly with set schedule (hybrid arrangement)
• Professional development and cross-functional training opportunities
• Equal Employment Opportunity employer