I have worked in the medical device industry for 12 years, predominantly in the quality sector, my areas of expertise are:
Technical documentation: authoring, proofreading and approval of various technical documents, such as; manuals, protocols/reports, SOPs, material/process/product specifications.
Quality Systems: requirements of ISO9001:2015, ISO13485:2016 & FDA CFR21: Part 820 and creation of documentation complying with these standards.
Computer Skills: Microsoft Word & Excel, data entry, database maintenance, data analysis (tracking and trending, compiling metrics), web search.
(I would be no help in logo design)
When are you looking to be ISO9001 certified?
Please don't hesitate to contact me if you feel I am suitable for your project.