Senior system validation specialist

Validation Expert

This is a critical role that will play a pivotal part in shaping and executing our validation strategy across the digital ecosystem.

* • Qualified engineers will contribute to the development and implementation of robust computerized system validation approaches, ensuring we meet global regulatory expectations while driving operational efficiency.
* • This position will be responsible for ongoing compliance throughout the Qualification & Validation (Q&V) lifecycle for both existing and new equipment, systems, and processes.
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About You

We are looking for degree holders in science, IT or engineering disciplines with demonstrable experience in computerized system validation within the pharmaceutical or biotechnology industry. The ideal candidate should have strong technical skills including work with GxP computerized systems; understanding of 21 CFR Part 11, EU Annex 11, and GAMP 5. Familiarity with diverse system types such as MES ERP LIMS QMS etc. And understanding of IT service management processes software development methodologies is essential.