Not specified (assumed to be on-site based on location)
Iso13485 and gmp compliance knowledge
Medical device regulatory familiarity
Statistical analysis for quality data
Johnson & Johnson is seeking a Quality Specialist to join their team in Suzhou, China, focusing on quality management and collaboration with cross-functional teams. The ideal candidate will have experience in quality systems and be familiar with medical device regulations
Job Summary
The role involves handling complaint investigations for Ethicon products and preparing detailed monthly, quarterly, and annual review reports.
Candidates will collaborate with cross-functional teams to monitor process capabilities and support factory projects from a quality perspective.
The position requires ensuring compliance with all applicable federal, state, local laws, and Johnson & Johnson company policies.
Matching Summary
Match Score: 80
Johnson & Johnson is seeking a Quality Specialist to join their team in Suzhou, China, focusing on quality management and collaboration with cross-functional teams. The ideal candidate will have experience in quality systems and be familiar with medical device regulations.
Skills & Requirements
Must-have
ISO13485 and GMP compliance knowledge
Medical device regulatory familiarity
Statistical analysis for quality data
Complaint investigation and reporting
Internal and external audit participation
Nice-to-have
Power BI and Power APP proficiency
SAP operational experience
Auto Flow software usage
Cross-functional collaboration skills
Process capability monitoring expertise
Key Requirements
Bachelor's degree in Medicine, Biology, or Chemistry
2-3 years of quality work experience preferred
Fluent English reading, writing, and speaking skills