Description
Our client is a pharmaceutical company and is looking for a Validation Engineer to take part to qualification/validation activities on manufacturing equipment. The Validation Engineer will work at our client in Belgium for at least 2 months.
Scope of work:
- Support qualification and process validation activities for revamping
- Tasks will be mainly to follow and document testing activities, to write qualification document (reports, traceability Matrix, update risk analysis), to update process validation protocols, prepare and follow validation activities, to analyze data's and prepare report.
- Project environment will be mainly in the chemical facility
- Qualification/Validation project following:
- Support project as Q/V SME
- To write qualification document
- To follow and document testing activities (testing for utilities/room/equipment)
- To write/update validation document
- To follow and document process validation activities (chemical process)
- To analyze and document results - Depending project scheduling and prioritization, activities could evolve.
Requirements:
- Engineer, min 3 year experienced in qualification/validation activities for pharmaceutical sector (immediate efficiency needed, no beginner)
- Qualification experienced and process validation knowledge is a must.
- Analytical, client and team spirit mindset
- Good knowledge of classical equipment used in chemical production
- Able to coordinate several qualification projects/activities in the same time
- Field oriented
Keywords: validation engineer, validation, ingénieur validation, qualification, validation, IQ, OQ, PQ, validation, qualification