Cleaning Validation (Atlanta, GA)

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          "text": "<ul><li>Cleaning Validation is a must </li><li>Expertise in “Risk Based Approach” for Commissioning and Qualification practices</li><li>Planning and Integration of Commissioning and Qualification activities in medical device manufacturing (Class II preferred)</li><li>Risk Management practices (i.e. Assessments, Functional Risk Documents, pFMEA, etc.)</li><li>Equipment qualification and process validation</li><li>Computerized System Validation (PLC, HMI, etc.)</li><li>21 CFR Part 11 requirements and how to incorporate these requirements into an efficient testing strategy</li><li>Assist in deviation investigation and resolution for problems and issues encountered during field execution activities</li></ul>",
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