GMP Quality Validation - Lab
External
Medvacon · Kansas City, MOPrepare for this interview
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About the role
Validation representative for laboratory validation activities, including Equipment Qualification and systems administration. In addition, provide technical guidance as a SME with respect to validation/process deviations and change controls as pertains to validation impact. This is on W2 only No expenses ONSITE SHIFT - M-F 8-4PM -DURATION 1 YEAR WITH OPTION TO EXTEND Bachelors in related Field or 2-10 years of Scientific or Engineering experience 3+ years work exp in project/process engineering and validation of FDA-covered processes, as well as QA experience in a pharmaceutical environment. Please attach a WORD resume to your submission All of your information will be kept confidential according to EEO guidelines. ON-SITE only This is a contract role and does not offer benfits 40-hour week 1 YEAR WITH OPTION TO EXTEND -
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