Technicien.ne Qa Opérationnel Process - Cdd 6 Mois
GSK
Wavre, Belgium
Document review and correction
Production floor support
Environmental monitoring reports
You will perform reading, correction, writing, and review of production-related documentation
Job Summary
You will perform reading, correction, writing, and review of production-related documentation.
You will provide on-site support for product quality maintenance and development, including oversights, gembas, management monitoring, and validation activities.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together.
Matching Summary
You will perform reading, correction, writing, and review of production-related documentation.
Skills & Requirements
Must-have
Document review and correction
Production floor support
Environmental monitoring reports
GMP compliance
SAP familiarity
Nice-to-have
Analytical skills
Resilience in complex situations
Organizational aptitude
Open to dialogue and tolerance
Risk assessment
Key Requirements
Bachelor's degree in scientific field or A2 diploma with 10+ years experience
Minimum 5 years biopharmaceutical production experience