Added
18 days ago
Type
Full time
Salary
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documentation validation manufacturing gmp process

📋 Description

  • Monitors equipment and manufacturing processes with minimal supervision
  • Sets up, cleans up, and maintains equipment
  • Reacts to unanticipated conditions and informs supervision
  • Observes quality characteristics of products and processes
  • Completes documentation per cGMP guidelines

🎯 Requirements

  • High School diploma required; Bachelor’s/Associate in science field desirable
  • Minimum 5 years manufacturing experience in pharma or similar
  • Experience with validation, troubleshooting and document management
  • Reading and following operating instructions and process flows
  • Ability to perform basic math and explain deviations clearly
  • Problem-solving skills and ability to work independently

🎁 Benefits

  • Comprehensive benefits package including PTO, medical/dental/vision
  • 401(k) plan and eligibility for short-term incentive programs
  • AbbVie Equal Opportunity Employer
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