OUR CLIENT: Meet is proud to partner with an innovative medical device company in the San Diego area developing novel devices for the biosurgery market.
THE POSITION: We're searching for a skilled Quality Assurance Specialist Contractor to assist with the preparation of documentation to improve compliance with regulatory standards (e.g. MDR, ISO 13485:2019). This includes the preparation of SOPs (Standard Operating Procedures), WIs (work instructions), DHF (Design History Files), policies, and any related quality documentation.
This is a 6-month contract expected to be 20 hours/week with potential to extend.
Bachelor’s degree in science related field (Chemistry, Biology or equivalent)
1-2 years of experience in cGMP manufacturing, Quality Control, or Quality Assurance
Technical writing experience: ability to write up SOPs and WI
Maintain records, spreadsheets, tables and other tracking documentation
Assist with technical writing of processes, practices, and methods
Excellent written and oral communication skills
Basic computer knowledge, including Microsoft Word and Excel
Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues
Meet Recruitment 2022. Meet Recruitment Ltd., Meet Recruitment Inc. and Meet Personalberatung GmbH are all subsidiaries of Meet Group (No. 13556131) a company registered in England and Wales at Irongate House, 22-30 Dukes Place, London, EC3A 7LP.