Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases while fostering an inclusive work environment that respects diversity and dignity
Job Summary
Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases while fostering an inclusive work environment that respects diversity and dignity.
The QA Specialist is responsible for GMP supervision, document auditing, safety management of special drugs, CAPA tracking, and training new QA staff to ensure compliance and quality in pharmaceutical production.
The role requires strong communication and collaboration skills, adherence to safety and environmental standards, and the ability to drive innovation and change within a multinational company environment.
Matching Summary
Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases while fostering an inclusive work environment that respects diversity and dignity.
Skills & Requirements
Must-have
GMP compliance and supervision
Production batch record review
CAPA management and closure
Safety management of special drugs
Document drafting and review
Training of QA personnel
Fluent English communication
Nice-to-have
Project management experience
Team collaboration and cross-departmental cooperation
Proficient with Windows and office software
Innovative and change-driven mindset
Strong sense of responsibility
Ability to handle market and compliance changes
Key Requirements
Bachelor degree or above in pharmaceutical, chemical, biochemical, or pharmaceutical engineering
5 years pharmaceutical industry experience
3 years multinational company experience
Fluent written and spoken English
GMP knowledge and experience
Experience in pharmaceutical and packaging processes