Description
The company
The Harvey Nash Group was founded in the UK in 1988, and now has offices throughout Europe, America and Asia. The Harvey Nash Group is known for the thousands of successful assignments completed throughout the world.
From more than 39 offices, and with 5000 staff and associates, we offer a unique range of consulting recruitment specialising in IT recruitment, benefits subcontracting and outsourcing services to our clients. Our departments of Executive Search and Interim Management support our customers around the world by placing the senior managers essential to business growth and effective management.
For one of our clients in the pharmaceutical sector, we are looking fora "Support QA validation et QA Local"
KEY RESPONSIBILITIES
- Critical review of all type of validation documents
- Review of deviations and CAPA before approval
- Review of tasks in Change control
- Review of work order linked to maintenance and production activities
- Interaction during shutdown
- Support during preparation of belgian inspection
- Participate during implementation of QIP activities ( autoclave, cleaning,...)
PREREQUISITES
Education: Engineering/pharmaceutical
Knowledge:
SAP if possible
GMP, Eudralex, CFR2 1, ...
Validation experience
Knowledge of quality systems
If possible already be in contact with similar gsk activities (knowledge os some local validations SOP)
Experience:
Minimum of 5 years of experience in pharmaceutical industry (validation, deviation, CAPA,...)