Validation Engineer - Ireland, Dublin - 9 Month Contract
Our client is a global leader in pharmaceutical innovation, specialising in the development and manufacture of cutting-edge drugs. As they continue to grow, they’re seeking an experienced Validation Engineer to join their dynamic team and drive forward groundbreaking projects in Dublin.
What you’ll do:
- 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.
What you’ll need:
- Extensive experience with a pharmaceutical or biotechnology company with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
- Bachelor’s degree (or higher) in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry etc.
- Experience in Facility, Utility and Equipment qualifications, examples include CTUs, Parts Washers, Autoclaves, Clean Utilities, Cleanrooms/HVACs etc.
- Prior experience with upstream cell culture and/or downstream formulation/fill finish processes.
If this role is of interest to you, please apply now!
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