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Manufacturing
Quality Inspector / Technician
West Greenwich, RI

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Planet Pharma Group

Associate Quality Assurance

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Job Description

Target PR Range:
19-28/hr
DOE Experience:
Associates degree at a minimum. Basic GMP experience, Document management experience, Familiar with working within a regulated industry, Strong attention to detail.
Job Details:
Responsible for the maintenance of all required documentation for the site under the direction of Quality Management with coaching from the Document Management Subject Matter Expert. Provide comprehensive services in accordance with Good Manufacturing Practices (GMP) within Document Management with ability to flex support as needed within the Quality System space.