Johnson & Johnson provides an inclusive work environment where each person is considered as an individual and respects diversity and dignity of employees
Job Summary
Johnson & Johnson provides an inclusive work environment where each person is considered as an individual and respects diversity and dignity of employees.
The role involves daily GMP supervision, document review, system management, safety management of special drugs, and training of QA personnel to ensure compliance and quality.
The position requires collaboration with multiple departments and adherence to safety, health, and environmental standards to maintain high-quality pharmaceutical production.
Matching Summary
Johnson & Johnson provides an inclusive work environment where each person is considered as an individual and respects diversity and dignity of employees.
Skills & Requirements
Must-have
GMP compliance and supervision
Production and packaging batch record review
CAPA management and closure
Safety management of special drugs
Document drafting and review
Training of QA personnel
SAP system maintenance
Nice-to-have
Project management experience
Collaboration and team spirit
Fluent written and spoken English
Innovative and change-driven mindset
Good communication and negotiation skills
Ability to adapt to market and compliance changes
Key Requirements
5 years pharmaceutical industry experience
3 years multinational company experience
Bachelor degree or above in pharmaceutical, chemical, biochemical, or pharmaceutical engineering