Medical Device 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 Format transferring of a sister company.
Principle Duties and Responsibilities:
The consultant will have experience with Technical Writing in the Life Sciences field. The client recently bought out sister company and looking to reformat the QA documentation (some may need completely overhauled). The resource must be proficient with QA documentation standards. 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
- QA Documentation
- Best Documentation Practices
Job Type: Contract