CQV Engineer

Pharmatek Consulting

Columbus, Ohio

JOB DETAILS
SKILLS
Capital Equipment, Commissioning, Documentation, Documentation Standards, Leadership, Process Development, Process Validation, Project Schedule, Risk Analysis, Technical Editing, Test Scripts, Testing, Validation Documentation
LOCATION
Columbus, Ohio
POSTED
30+ days ago

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


About the Company

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Pharmatek Consulting