Validation Specialist

Validation Specialist – Pharma / Biopharma – Permanent – South East Our client is a leading life science organisation. At present, they are seeking a Validation Specialist on a permanent basis at their site in the South East, UK. Responsibilities: To co-ordinate and execute the validation and re-qualification of facilities, processes, equipment, and Computer Systems (including cleaning validation) where required, to meet the site operations business needs. Deliverables: – Ensure review and update of validation procedures (Policies, Master plans, SOP’s etc.) for equipment and facilities – Establish and maintain Validation Plans as applicable – To prepare, execute and report validation protocol including cleaning validation in accordance with EU GMP – To perform qualification and requalification temperature mapping activities of storage locations, i.e. refrigerators, freezers and incubators – To perform qualification studies on other equipment and processes – Establish and maintain the re-qualification schedule for validated equipment – Liaise with Engineering, Quality Assurance and User Departments to ensure that validation is conducted in a timely manner according to the Validation Plan and with minimal disruption to production – Attend meetings, both internal and external, representing the department in a professional manner – Participate in audits by customers and regulatory authorities – To ensure that safe working methods and…