Techncial writer is required for a leading medical device company based in Limerick. The companies FDA regulated Limerick facility has grown consistently over the last 20 years to become one of the most important sites in its global operations. This facility specialises in the production of disposable contact lenses in a state of the art operation which includes injection moulding, robotics, vision systems and sterilisation systems in a Class 100,000 cleanroom environment. The facility has over 50 fully automated manufacturing lines and the product is untouched by a human hand from start to finish of the process.
If you are looking for an opportunity to work in a leading edge medical device facility with a focus on process innovation, automation and continuous improvement with steady personal growth and development opportunities then call us to find out more.
In this role you would provide support for the technical/validation documentation and support activities within engineering to ensure that all activities associated with change control and general Engineering support tasks are completed in a fully compliant manner in accordance with the requirements of the clients Validation/Quality Policies and Procedures. The role requires collaboration with Quality Engineering to ensure Validation/Quality Policies and Procedures are maintained.
Perform technical writing, research, and related editing functions to prepare documents, test plans, user cases, project manuals, business proposals, reports, briefings, presentations, guidelines, and other written materials.
If this role is of interest, please call Regina at LSC on 021 4777 329 or apply directly through this advert