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M
GMP Quality Validation - Lab
MEDVACON · Kansas City, MO, United States
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
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- 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.
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- 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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