Description
Validation Engineer - Contract - BelgiumA major Biotechnology/Pharmaceutical organization has a fantastic opportunity for a fluent Dutch and English speaking Validation Engineer to join the team based in Belgium. The Validation Engineer will be responsible for the qualification of process systems ie production equipment & utilities.
The Role:
.Set the validation documents according to current FDA and European regulations and recent industry standards.
.Make sure the entire validation life cycle in accordance with the procedures of the organization which includes validating input in the preparation of user requirements (URS), implementation of the System Impact Assessments and the subsequent validation activities (DQ, IQ, OQ, PQ) release of the system to the end user.
.Other duties include validation activities in the context of change control and periodic review of the role.
Experience:
.Bachelor`s or master`s degree, preferably in a scientific discipline
.Several years of experience in a quality role
.Familiar with the cGMP regulations and relevant industry standards
.Team player with strong analytical and problem-solving abilities.
.Results oriented, flexible and can work independently
.Fluent in Dutch and English
An outstanding daily rate is on offer alongside an exceptional opportunity to join a major Biotechnology/pharmaceutical organization.
Please apply today with a covering letter highlighting your key skills and relevant experience aligned to this contract opportunity