Career Opportunity: CSV Validation Engineer
Job Description:
We are seeking a skilled and experienced CSV Validation Engineer to join our team. As a key member of the Automation team, you will play a crucial role in ensuring the validation of CSVs within a Pharmaceutical environment.
Responsibilities:
* Act as the Subject Matter Expert (SME) for CSV-related activities and projects
* Participate and lead CSV activities linked to Automation projects
* Support the preparation of Gx P Computerised System Lifecycle documents, including validation plans, requirement specifications, risk assessments, qualification protocols, requirements traceability matrices, and validation reports
* Design, generate, and execute test plans and test protocols, managing and reporting findings and non-conformances raised during all types of testing
Requirements:
To be successful in this role, you will require:
* A third-level qualification in Electrical, Electronic, Systems Engineering, Computer Science or equivalent
* At least 5 years of experience working in control systems validation in the Life Sciences/Pharma sector
* Excellent communication and technical writing skills
* Experience of PLC/SCADA and OSIsoft PI Data Historian Validation
Benefits:
This is a site-based role with excellent opportunities for career development and growth. You will have the chance to work with a talented team of professionals and contribute to the success of our organization.