Quality Assurance Specialist

138675
  • Competitive
  • San Diego, United States
  • Contract
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.

REQUIREMENTS:
  • 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
Jamie Zogaric Recruiter

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