CQV Engineer

Pharmatek Consulting

  • Columbus, Ohio
  • 30+ days ago

    Highlights

    Completing user interface testing, software verification, and complete alarm testing on automated systems. Demonstrated experience in leading CQV activities specific to Process Equipment.

    Numbers & Facts

    LocationColumbus, Ohio
    Websitewww.consultpharmatek.com

    Description

    Full time role

    CQV Engineer

    Columbus OH, Onsite

     

    CQV Engineer Responsibilities:

    • Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of a 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
    • Documenting impact and risk assessments as part of a team
    • Completing user interface testing, software verification, and complete alarm testing on automated systems
    • Developing, reviewing, and executing testing documentation
    • Making recommendations for design or process modification based on test results when executing test scripts
    • General understanding of capital equipment implementation and process knowledge
    • Understanding validation documents, URS, IQ, OQ, PQ

     


    Requirements

    • Must be willing to work onsite in Columbus, OH
    • Bachelor’s Degree or equivalent required
    • Demonstrated experience in leading CQV activities specific to Process Equipment


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