Description
Ekco is hiring an experienced Technical Writer to author, review, update, and maintain IT standard operating procedures, work instructions, qualification documentation, and templates in a GxP-regulated pharmaceutical environment. The role covers IT change and release management, incident and service management, backup and recovery, patching, configuration, audit trails, cloud and supplier controls, data integrity, ITIL and ITSM documentation, document lifecycle management, regulatory inspection support, and training. Candidates need at least three years of controlled-documentation experience in pharmaceutical, biotech, or medical-device industries, with IT or computerised-systems experience, plus knowledge of 21 CFR Part 11, EU Annex 11, GAMP 5, data integrity, ITIL, and relevant EDMS and ITSM tools.
