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Principal Validation Specialist

3 weeks ago

Galway, Galway, Ireland beBeeValidation Full time
Senior Validation Engineer

We are seeking an experienced Senior Validation Engineer to join our team on a contract basis. The successful candidate will be responsible for developing and approving validation documentation, including protocols, records, and reports.

The ideal candidate will have a strong understanding of current Good Manufacturing Practices (GMPs) and 21 CFR 820 requirements, as well as excellent analytical and interpersonal skills.

  • Develop, approve, and maintain validation documentation, including protocols, records, and reports.
  • Perform and oversee process and test method validation activities within the project.
  • Communicate with functional groups to ensure awareness of validation requirements.
  • Investigate and troubleshoot validation problems which may occur and determine solutions.
Required Skills and Qualifications

To be considered for this role, you will need:

  • A bachelor's degree in an engineering, technology, or scientific discipline.
  • At least 5 years' experience in the medical device or pharmaceutical industry.
  • Prior experience in the design and execution of process and test method validations.
  • Strong analytical and interpersonal skills.

This is a fantastic opportunity to work on a challenging project and develop your skills as a Senior Validation Engineer. If you are a motivated and organized individual with a passion for validation, we encourage you to apply for this exciting role.