Here is a brief job description:
The Technical Writer III role will be responsible for writing EU Medical Device Directive 2.7.1 rev 4 compliant Clinical Evaluation Reports and associated documents, templates, and processes.
If a candidate has this specific experience they will be a fit for the role as the experience will already be in place based off of doing this type of work before.
I look forward to hearing from you
APN Software Services, Inc .
39899 Balentine Drive, Suite 385, Newark, CA 94560 .
Direct: 510.623.5049 | Fax: 510.623.5055 | Email: email@example.com