R&D Assay Documentation & QA Submissions Specialist
Listed on 2026-09-22
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Quality Assurance - QA/QC
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Healthcare
Tempus AI is seeking a documentation specialist to support IVD regulatory submissions. You will draft, edit, and maintain GMP/ISO-compliant documents for the molecular R&D group and collaborate with scientists, technologists, and QA/regulatory professionals.
The role emphasizes meticulous record-keeping, version control, and audit preparation in a fast-paced environment. A Bachelor’s degree plus 2+ years in medical device documentation is expected.
We invite applications for the R&D Assay Documentation & QA Submissions Specialist position located in IL, United States.
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