Validation Expert Job Opportunity
Join a leading Biopharmaceutical organization based in Ireland to discover an exciting career opportunity.
As a Validation Expert, you will be responsible for executing qualification and validation activities for life cycle approach following validation plans and complying with cGMP and company procedures. This includes design, build, qualification, and ongoing operations to maintain the validated state.
* Author, review, execution, and approval of testing protocols and reports.
* Participate on project teams, vendor enquiries, troubleshooting, and monitoring of process systems.
The ideal candidate will have:
* A minimum of 3-5 years' experience working in a pharmaceutical or similar GMP environment as part of a validation, MSAT, or engineering function.
* Experience in commissioning and qualification/validation of facilities, utilities, equipment, and instruments (e.g., bioreactors, chromatography, ultrafiltration, autoclaves, parts washers).
* Experience in maintaining the validated state, requalification/revalidation (CTUs, Cleanrooms, Clean Equipment etc.).
This is an excellent opportunity for motivated professionals looking to join a multinational organization who are one of the best at what they do.
We offer a challenging and rewarding career path with opportunities for growth and development.