Job description:
Our client is looking to bring on an equipment validation consultant for a 6 month project (extensions likely). This Consultant will be responsible for drafting and executing IQ, OQ protocols, work with their equipment and complete summary reports. This person needs to be able to both write and execute validation protocols. They will also be writing Validation Documents such as URS, FDS. The client already has SOP’s in place, so the consultant will be writing these protocols and reports in accordance with the client’s SOP’s. Candidates who have Kaye Validator working knowledge is preferred for temperature mapping purposes. MUST BE able to work independently with a minimal supervision.
Skills:
Equipment Validation, Writing/executing protocols, Validation Summary reports, Drug Product/Drug delivery systems
Education Requirements:
B.S. in science or engineering preferred
MA: Validation Engineer (232389)
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