Freelance CQV Engineer

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  • Create validation plans.
  • Perform and document impact and risk assessments, evaluating direct, indirect, and non-impact systems in complex processes.
  • Maintain detailed records of qualification, validation, and change control activities for compliance audits.
  • Write, edit, and execute technical commissioning, qualification, and validation documentation for equipment, systems, software, and processes under project leader guidance.
  • Run test scripts and document results.
  • Adhere to project schedules for assigned tasks.
  • Conduct user interface testing, software verification, and alarm testing on automated systems.
  • Develop, review, and execute testing documentation.
  • Recommend design or process modifications based on test results.
  • Understand validation documents, URS, IQ, OQ, and PQ.

Your profile:

  • 5-7 years of proven CQV experience in GMP-regulated environments.
  • Must have experience in Cleaning Validation.
  • Strong business maturity and interpersonal skills for effective communication and collaboration.
  • Ability to clearly communicate requirements with rationale to various levels within the client’s organization.
  • Demonstrated attention to detail and organization in project work.
  • Ability to work independently on assigned tasks.
  • Training in GMP and Good Documentation Practice (can be completed during onboarding).
  • Intermediate proficiency in WORD (creating/editing large technical documents with styles, tables, TOCs, track changes).
  • Basic proficiency in EXCEL and PowerPoint.
  • Strong interpersonal skills and clear communication abilities.

    If you are interested please send your CV to

Darwin Recruitment is acting as an Employment Business in relation to this vacancy.

James Gregory

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