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FSP QA Auditor I @ Thermo Fisher

Worcester, Massachusetts, USOnsiteFull-time
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About this role

Embrace the opportunity to become a QA Auditor I and play a vital role in ensuring GMP compliance and quality in clinical auditing. Support specification revisions, document control, and cross-functional collaboration while advancing your career in a dynamic, innovative environment. Grow your expertise with industry-leading tools and make a real impact on product excellence.. Category: Quality & Regulatory

Skills

gmp compliancespecification revision managementdocument controlbatch record reviewgxp compliancemicrosoft office suiteonetrackonevaultsamplemanagerrisk assessmentimpact analysisconflict managementschedule adherenceindependent work

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