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Support the site validation activities across a number of workstreams. Support site EMPQ strategy and implement/maintain EM protocols and procedures for graded pharmaceutical areas, ensuring compliance with regulatory guidelines. Support equipment qualification post Operational Qualification (OQ) through to Process Performance Qualification (PPQ) and subsequent requalification/revalidation. Support global regulatory submissions, internal audits and external inspections/audits as needed. Facilitate problem solving & risk assessment p...
About the Role
Validation Engineer
RK26014
Contract 6 months
Louth
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Louth. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Key Responsibilities:
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