What are the responsibilities and job description for the QA Analyst position at PRIDE Health?
The Science Team with Russell Tobin & Associates is hiring a QA associate to support our client’s research facility based in South San Francisco!
This is a 10 month contract opportunity with potential for extension or conversion.
M-F 8a-5p
Job Responsibilities:
Management and continuous improvement of Monogram’s Quality Management System under the guidance of the QA Manager or Director.
Management and continuous improvement of paper and electronic quality systems in compliance with QSR, CLIA, GxP and other applicable regulations and guidelines.
Management and maintenance of Monogram’s document control system; processing and technical editing of QA controlled documents (e.g. SOPs, Forms, Policies) including project/product-specific documents.
Trending and analysis of key quality metrics including nonconformance data. Review and tracking of CAPA action items. Assisting in the investigations and determination of root cause.
Qualifications:
Associate or B.S. degree in a scientific discipline with 4-6 years of hands-on Quality or related experience in a regulated environment, preferably in Part 820 QSR, ISO 13485, medical device, GxP or CAP/CLIA.
Knowledge of US GxP compliance regulations and industry practices, as well as EU GxP requirements.
Must possess strong technical documentation skills.
Additional Information:
RTA is unable to offer visa sponsorship now or in the future
RTA is able to offer benefits after 60 days of employment
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