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Document Reviewer II - QA - Afternoon @ Thermo Fisher

Whitby, Ontario, CAOnsiteFull-time
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About this role

Embrace the opportunity to become a Document Reviewer II - QA and play a key role in ensuring data integrity and compliance in pharmaceutical analysis. Utilize your expertise in GMP, LIMS, and analytical techniques to review critical documents and support laboratory operations. Grow your career in a collaborative, safety-focused environment with opportunities for continuous improvement.. Category: Research & Development

Skills

good manufacturing practicesanalytical developmentlims softwaretrackwiseempowernugenensishigh performance liquid chromatographygas chromatographyultraviolet spectroscopytitrationsop writingchange controlmicrosoft officedetail orientationdeadline management

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