Medical Device Quality Tech Writer
Medical Device QA Technical Writer
Our client is a small medical device manufacturer. They develop and manufacture a number of orthopedic devices. They are in need of a QA Technical Writer to come in and support our client’ s ISO 13485 certification, as well as a new acquisition.
Principle Duties and Responsibilities:
The consultant will have experience with Technical Writing in the Life Sciences field. The client is currently seeking their ISO 13485: 2016 certification, and will need an individual who can help support the writing of QA documentation (some from scratch). The resource must be proficient in the related ISO 13485 standards and related 21 CFR 820 regulatory subchapters.
This person needs to have experience writing SOP’ s, Work Instructions, and Quality Documentation.
- Medical Device
- Technical Writing
- ISO 13845: 2016
- Best Documentation Practices
Job Type: Contract