Post Market Surveillance Manager
Core
Overseeing post-market surveillance processes, enhancing reporting systems, managing team talent, and investigating product complaints to ensure regulatory compliance for medical devices.
Role type
Post Market Surveillance Manager
Builds
Regulatory compliance frameworks, reporting tools, and team capabilities for medical device safety.
Domain
Medical Devices / Regulatory Affairs
Deliverable
client delivery
Required skills
Post Market Surveillance Operations, Medical Device regulations, Quality Assurance, Quality Control, Clinical Research, Team Leadership, Process Improvement, Statistical Methods, Adverse Event Reporting, Risk Management, Recall Management
Preferred skills
None stated
Technologies
None stated
Responsibilities
Oversee implementation of post-market surveillance processes and ensure adherence to standards; Review and enhance reporting systems for timely and accurate data; Manage talent including selection, performance, compensation, and career development; Design training programs on regulatory compliance and risk management; Conduct quality assurance assessments on communication tools; Lead medium to large scale process improvement efforts.
Seniority
Manager, direct and indirect reports
