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Job Location | Hamilton |
Education | Not Mentioned |
Salary | Not Mentioned |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent |
Fusion Pharmaceuticals (NASDAQ: FUSN) is a clinical-stage oncology company focused on developing next-generation radiopharmaceuticals as precision medicines. Fusion connects alpha particle emitting isotopes to various targeting molecules to selectively deliver the alpha emitting payloads to tumors. Fusion #39;s clinical portfolio includes: FPI-2265 targeting prostate specific membrane antigen (PSMA) for metastatic castration resistant prostate cancer currently in a Phase 2 trial; FPI-1434 targeting insulin-like growth factor 1 receptor currently in a Phase 1 trial; and FPI-2059, a small molecule targeting neurotensin receptor 1 (NTSR1), currently in a Phase 1 trial. In addition to a robust proprietary pipeline, Fusion has a collaboration with AstraZeneca to jointly develop novel targeted alpha therapies (TATs) and combination programs between Fusion #39;s TATs and AstraZeneca #39;s DNA Damage Response Inhibitors (DDRis) and immune-oncology agents. Fusion has also entered into a collaboration with Merck to evaluate FPI-1434 in combination with Merck #39;s KEYTRUDA (pembrolizumab) in patients with solid tumors expressing IGF-1R. To support Fusion #39;s growing pipeline of TATs, the company has signed strategic actinium supply agreements with TRIUMF, Niowave, and BWXT Medical.Position SummaryFusion has opened a newly created role in Quality Assurance for a Document Control Specialist I. The Document Control Specialist I will be responsible for processing and managing documents from initiation to release in the Veeva QualityDocs eDMS. This person will also be responsible for issuing batch records, worksheets, logbooks, and other requested documents to support an array of departments such as QC, Manufacturing, and Quality Assurance. This role will report to the Director or Associate Director of Site Quality.Key Responsibilities