Validation Engineer

Morgan McKinley View all jobs

  • Carlow
  • Contract
  • Full-time
  • 2 months ago
We are looking for a Validation Engineer to join our client, a leading Biopharmaceutical company in Carlow for a 12 month hourly rate contract.Key Responsibilities
  • Project validation support including conducting equipment performance qualifications (specifically cleaning and sterilization validation)
  • Authoring project validation master plans; SOP and documentation updates; Authoring validation protocols and final reports, executing validation studies, analysis of validation data; Resolving technical issues encountered during study execution.
  • This individual will be required to work in a cross-functional team and independently to accomplish validation project objectives.
  • Works with moderate work direction and is skilled and knowledgeable to the position.
Skills, Attributes & Experience
  • Degree in Engineering or a Scientific related discipline.
  • Minimum of 3 years + experience working in a Validation role within Pharmaceuticals or Medical Device.
  • Equipment Validation and Sterilization Validation experience.
  • The successful candidate must have strong technical writing and oral communication skills.

Morgan McKinley

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