Pharmaceutical Validation Professional

2 weeks ago


Cork, Cork, Ireland Elusav Recruitment Full time
About the Role

We are seeking a highly skilled CQV Engineer to join our client's team in Ireland.

The successful candidate will be responsible for supporting new product introductions, equipment qualification, and the site requalification program.

Main Responsibilities
  • Designing, executing, and reporting on PV/Process Performance Qualifications.
  • Designing, executing, and reporting on validation studies for equipment, systems, and processes.
  • Ensuring validation studies are managed in conjunction with all required standards and legal requirements (Health & Safety, cGMP, construction, environmental etc.).
  • Providing technical interpretation and guidance of current US FDA and EU validation requirements for aseptic processing, lyophilisation, sterilisation, and depyrogenation.
Requirements
  • 3-5 years' experience working in a Healthcare manufacturing environment – ideally part of which would be in the pharmaceutical sector.
  • A degree in Science (Chemistry, Micro., or Pharmacy preferred) or Engineering Chemical/Mech/Elec).
  • Capable of troubleshooting validation issues associated with projects, process development etc.
  • Competent technical knowledge of pharmaceutical plants.

The ideal candidate will possess excellent communication skills, both written and verbal, and be able to work effectively at organisation, team, and individual levels.



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