Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases while fostering an inclusive and diverse work environment
Job Summary
Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases while fostering an inclusive and diverse work environment.
The QA Specialist is responsible for daily GMP supervision, document audits, system management, safety management of special drugs, and cross-departmental collaboration to ensure compliance and quality.
The role requires a proactive attitude with a strong sense of responsibility, flexibility to work under tight deadlines, and the ability to drive innovation and teamwork.
Matching Summary
Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases while fostering an inclusive and diverse work environment.
Skills & Requirements
Must-have
GMP compliance and supervision
Document and batch record review
Production site quality management
CAPA and complaint handling
Safety management for special drugs
Training and qualification certification
Fluent English communication
Nice-to-have
Project management experience
Collaboration and team spirit
Adaptability and self-awareness
Innovative and change-driven mindset
Good communication and negotiation skills
Proficient in Windows and office software
Fluent in Chinese (ideal)
Key Requirements
5 years pharmaceutical industry experience
3 years multinational company experience
Bachelor degree or above in pharmaceutical, chemical, biochemical, or pharmaceutical engineering
Fluent written and spoken English
GMP knowledge and production site management experience
Experience with quality control and internal audits