QC Documentation Consultant
Liège – Contracting
#QC #documentation #procedures #process #lab #GMP #pharma
Our partner is currently looking for a QC Documentation Consultant. Our partner is a pharmaceutical company.
What are your responsibilities?
As a QC Documentation Consultant, you will participate to a global integration process by helping the quality control team in the implementation global procedure in the current local system, delivering according to plan, supporting other documentation/process activities to driving QC targets adherence. To be successful in this role, here are your main tasks:
- Reviewing global and local procedures to align them
- Works with QC lab team to identify business impacts.
- Adapt laboratory documentation.
- Evaluate training impact
- Reviews different QC documentation
- Work in collaboration with QA department
- Work in collaboration with global
Who are you?
You have experience in quality control in a GMP environment. You have experience in procedure review and creation. You speak fluently French and have at least an intermediate level in English. You are team oriented, a problem-solver and you learn quickly.
What can you expect?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.
You’re interested in this job? We kindly invite you to apply. Do you have any questions? You can contact Marie Defruit, [email protected].
