Senior QA Engineer - cGMP Validation in Nuclear Medicine
Listed on 2026-09-30
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Pharmaceutical
Quality Engineering, Regulatory Compliance Specialist
CT19 is seeking a Senior Quality Assurance Engineer to lead commissioning, qualification, and validation for a first-of-a-kind nuclear medicine production facility. You will own Master Validation Plan activities, oversee C&Q across equipment, utilities and processes, and drive validation reports in a highly regulated environment.
Ideal candidates have 5+ years in QA/validation within cgmp pharma manufacturing, deep knowledge of 21 CFR and cGMP, and experience with C&Q programs.
We would love to welcome a new Senior QA Engineer - cGMP Validation in Nuclear Medicine to our group in WI, United States.
The advertised compensation is 110..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior QA Engineer - cGMP Validation in Nuclear Medicine role in the description above.
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