Quality Engineer - PMS
Stryker(25 days ago)
About this role
A mid-level Post-Market Surveillance (PMS) Specialist in the medical device sector responsible for supporting complaint intake and regulatory reporting processes. The role ensures adherence to US FDA, EU MDR, and ISO 13485 standards while collaborating with cross-functional, geographically distributed teams in a hybrid work model.
Required Skills
- Complaint Handling
- Post-Market Surveillance
- Regulatory Reporting
- TrackWise
- Microsoft Project
- Quality Management
- Risk Management
- Communication
- Analytical
Qualifications
- BE/BTech
- ME/MTech
- ISO 13485:2016 certification
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