QA Specialist
Danaher · Zhejiang, China
The apply link worked recently (not employer-confirmed).
Role summary
Cytiva seeks a QA Specialist to manage document control, training systems, and quality workflows at its Tonglu facility. The role involves supporting audits, non-conformances, corrective actions, and internal quality issues while assisting manufacturing teams. Candidates need 2–3 years of QA experience, familiarity with ISO standards for medical devices, and proficiency in quality improvement methodologies.
What they're looking for
- Bachelor's degree in manufacturing or related field
- 2-3 years quality assurance and quality management system experience
- Knowledge of ISO 9001 and ISO 13485 medical device standards
- Proficiency with CAPA processes and QC 7 tools or lean six sigma
- CET-4 English certification with strong communication abilities
- Competency in Word, Excel, PowerPoint and similar office software
- Strong organizational, coordination and problem-solving capabilities
What you'll be doing
- Manage QA document control systems and coordinate site quality training delivery
- Support audit execution, non-conformance tracking, change control and CAPA workflows
- Assist manufacturing and CHU teams with internal quality issues and customer complaints
- Facilitate internal and external audit support activities
- Execute additional quality management tasks as directed by QA manager
Privacy & handoff
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