AVS is looking for a Computer System Validation (CSV) resource for work in a bioPharma facility. This is a long term position. A person in this role will perform the following duties: Write, review, and approval of validation SOPs and documentation for a PLC/SCADA based system. Maintain accurate validation documentation.  Train other staff members on the correct use of computerized systems in line with protocols and regulations.  Review and analyze validation data – compiling reports when required.  Involvement in both internal audits and external inspections as required.