I am new to the world of freelancing and due to this I am prepared to complete this job for a reduced fee and a positive recommendation on my profile if you are satisfied with my work.
I have worked in the medical device industry for 12 years, predominantly in the quality sector, where accuracy, efficiency and meeting deadlines are critical.
My main 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 Assurance: batch record review for product release, internal/supplier auditing and facilitating regulatory body audits.
Computer Skills: Microsoft Word & Excel, data entry, database maintenance, data analysis (tracking and trending, compiling metrics), web search.
Quality Systems: CAPA, NCs, complaints, manufacturing deviations.
I have completed many quality system audits, and compiled the subsequent audit report. I am also a certified ISO13485:2016 Lead Auditor.
Please don't hesitate to contact me if my auditing experience is applicable to your project.
Thanks
Stephanie