Post Market Surveillance Supv
IntuitiveBengaluruFull TimeEngineering
Remotely
regulatory complianceregulatory reportingmedical devicevigilancemdrcapa
Job Description
📋 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
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