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Senior Validation Engineer — GMP Radiopharma CQV
Job in
Indianapolis, Hamilton County, Indiana, 46262, USA
Listed on 2026-07-25
Listing for:
Bristol Myers Squibb
Full Time
position Listed on 2026-07-25
Job specializations:
-
Engineering
Pharma Engineer, Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Rayze Bio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Senior Validation Engineer to support a radiopharmaceutical facility in Indianapolis. You will draft and execute CQV documents for GMP spaces, collaborate with project teams, and help drive continuous improvement from construction through GMP operations.
The role requires 4–8 years in Radiopharmaceutical GMP manufacturing and validation, strong technical writing, and the ability to lead validation projects while coordinating
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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