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6348 - Validation Engineer / CQV Engineer

Verista, Inc.

Columbus, OH • On-site

Full-time

Posted 2 days ago

New


Job description

Validation/CQV Engineer Responsibilities:

  • Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader
  • Running test scripts and documenting results
  • Adherence with project schedule for all assigned activities
  • Maintaining clear, detailed records qualification and validation
  • Reading technical schematics to identify, locate, and test photo sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment

Requirements:

  • Bachelor's Degree or equivalent required
  • Prior experience supporting validation, qualification, or testing activities for packaging equipment or packaging lines preferred
  • Experience working in or supporting pharmaceutical, medical device, combination product, or regulated packaging operations is a plus
  • Proficiency using PC and Microsoft Office tools
  • Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
  • Ability to work as part of a team
  • Strong problem-solving and critical thinking skills
  • Excellent organizational and time management skills
  • Strong attention to detail
  • GMP and Good Documentation Practice training (may be completed at onboarding)
  • Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes)
  • Basic skills with EXCEL and PowerPoint
  • Strong interpersonal skills and clear communication capabilities