QA Supervisor
Core
Manage GSP-related policy and compliance affairs for Cytiva medical devices in China, support localization projects from a quality perspective, and lead post-market QA activities and audits.
Role type
QA Supervisor (Medical Devices)
Builds
Quality management systems and compliance frameworks for medical devices in China
Domain
Medical Devices / Life Sciences / Regulatory Compliance
Required skills
GSP compliance, GMP knowledge, ISO9001/13485 familiarity, problem solving, Quality Agreement management
Preferred skills
Internal auditor qualification (ISO9001/13485), cross-functional collaboration
Technologies
GSP, GMP, ISO9001, ISO13485
Responsibilities
Manage GSP-related policy and compliance affairs, support localization projects from a quality perspective, lead or contribute to post-market QA activities and audits, provide and review Quality Agreements
Seniority
Mid-Senior, hands-on IC