Description
Job Description:Description of the Job Duties
* Write and maintain user documentation for implantable medical devices
o Collaborate with and interview Subject Matter Experts (SMEs) to gather content for document creation.
o Facilitate review meetings of draft and final documentation with SMEs
o Follow Standard Operating Procedures for Document Creation
o Adhere to FDA and TUV standards
* Assist with the creation of a Style Guide for Directions for Use
* Perform Change Management tasks, such as creating Change Requests to approve and release documentation within an online documentation management system
* Manage translation of documentation using an outside vendor, including review of deliverables for any possible Quality issues
List of Education/Experience/ Skills necessary to do the job:
Advanced Proficiency with Adobe InDesign, Adobe Acrobat, Microsoft Word
At least two years of technical writing experience creating user documentation (writing samples required)
Preferred: English, Journalism, or similar degree
Preferred: Experience in a Regulated industry, preferably Medical Devices
Quality Systems Duties and Responsibilities:
Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
Please be in contact as soon as possible for this urgent position.
To find out more about Real please visit www.realstaffing.com