Post-Market Quality Lead: CAPA & Regulatory Strategy

A leading medical device firm located in San Diego, California is seeking a seasoned Quality Assurance professional to oversee post-market quality processes, including CAPA management and risk assessments. The ideal candidate must hold a Bachelor's Degree in a relevant field and have a minimum of 7 years experience in medical device QA. The role offers a competitive salary range of $155,900 to $257,300 annually and focuses on driving continuous improvement and regulatory compliance.
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