Deviation & CAPA Specialist
Walloon Brabant – Contracting
#deviation #capa #QA #quality #qualitysystems #continuousimprovement #GMP #pharma
You have a previous experience in the pharmaceutical industry? You have a good knowledge of GxP? You are solutions oriented? Keep reading the description of your future job!
Our partner is currently looking for a Deviation & CAPA Specialist to reinforce its teams. Our partner is a pharmaceutical company.
What are your responsibilities?
As a Deviation & CAPA Consultant, you will be in charge of the creation (if necessary), follow-up and closing deviations and CAPA. You will ensure Quality Oversight on the application of the systems by large and diversified operational area. To be successful in this role, here are your main tasks:
- Manage and Coordinate activities related to Deviation and CAPA Quality Systems.
- Manage and Coordinate continuous improvement of Deviations and Capa Systems and ensures processes are optimized in terms of compliance and efficiency.
- Contribute to the decreased in the number deviations and CAPA of the unit.
- Ensure that major issues with impact on quality system are captured, followed up and treated in site action plans.
Who are you?
You have a university degree in sciences. You have a relevant experience in the pharmaceutical industry (production, validation or quality assurance). You have a relevant experience in GxP. You speak fluently French. You have good interpersonal skills. You are a problem solver and a real team player.
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].