We are currently looking for an experienced Technical Author to up-revision, complete manufacturing and service documentation to regulatory compliant standards and product release timescales.
Responsibilities: creating and managing manufacturing and service documents working to FDA requirements in the medical equipment industry understanding and creation of IQ, OQ, PQ protocols and reports ability to drive documentation completion through regulatory processes monitoring, tracking and release of documents/DMR's across all functions close liaison with QA/RA and Service/Manufacturing engineers to ensure requirements have been correctly captured in documents producing best practice, world class documentation and to be able to provide recent examples of their own work
The successful candidate will have: Excellent and demonstrable technical documentation skills Excellent command of technical English Experience in creating Medical Equipment/FDA compliant documentation Excellent communication skills Ability to understand process descriptions and process maps and to convert these into simple, understandable process instructions Understanding of and experience in using State-Of-The-Art document creation software, techniques, tools and best practices Understanding of and experience in using web-page-based documentation delivery
Job Reference: JE15719
Closing Date: 08-Aug-2012