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GMP Quality Validation - Lab

MEDVACON · Kansas City, MO, United States

Diagnostics / LaboratorySenior LevelQuick applycontract27 days ago

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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