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Location: Hoofddorp (North Holland)
Duration: 9 months contract (extension is possible)
Working: Full time (40 hours)

Our client is one of the leading companies in biopharmaceutical industry, commited to promote new ways of treatment in serious diseases by developing innovative immunotherapies.

About the role
As a Quality Engineer you will act as a Quality reviewer/approver for Validation Deliverables related to facilities, Utilities and Equipment.

-Quality Validation SME for projects and changes related to facilities, Utilities and Equipment.
-Creating, reviewing, approving Validation deliverables for multiple projects related to facilities, Utilities and Equipment.

Preffered requirements
-Minimum 5 Years experience in Validation/Quality Role in GMP environment.
-Fully comfortable with general expectations for the execution of Validation deliverables.
-Fully understands the concept of a company quality system and the need to work within that system.
-Experience in Deviations, Capas, Change Control.
-In depth knowledge of GMP regulations/guidances/standards.
-Able to communicate clearly as a member of a cross functional team.