Remotely
quality assurancerisk managementregulatory compliancedesign controliso 13485iso 14971quality system21 cfr 820
Job Description
📋 Description
- QA lead for design transfer and change management in medical devices and combination products.
- Represent QA on cross-functional teams; ensure regulatory compliance worldwide.
🎯 Requirements
- Bachelor’s degree in engineering, science or technical field
- 6+ years in medical device, 4+ years QA experience
- Regulatory knowledge: 21 CFR 820, EU MDR 2017/745, ISO 13485, ISO 14971
- Design Control per 21 CFR 820.30; risk management and design change control
- Strong communication, leadership, and cross-cultural collaboration
- Product development experience and design history file/risk management oversight
🎁 Benefits
- Not specified in description