QMS Quality Engineer
Cepheid(1 month ago)
About this role
This role ensures the establishment, implementation, maintenance, and continual improvement of the company’s quality management system to meet medical device regulatory requirements (e.g., China GMP, ISO 13485). The position supports alignment with global headquarters and cross-functional stakeholders to ensure regulatory compliance and system effectiveness.
Required Skills
- Quality Management
- ISO13485
- GMP
- Auditing
- CAPA
- Document Control
- Training
- Regulatory Compliance
- Process Improvement
About Cepheid
cepheid.comCepheid is delivering a better way to improve patient outcomes by enabling access to molecular diagnostic testing everywhere.
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