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Details

QA Validation CSV Specialist / Snr Specialist


Reference:POR807431 Location: Limerick
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Validation Specialist

A QA Validation CSV Specialist or Senior Specialist is required to join a rapidly expanding global Biopharmaceutical business in Limerick. The main focus of this role is to implement policies and procedures to validate/qualify computer systems. You will plans, coordinate, and participate in a compliant validation process for quality information technology systems which require formal validation documentation under appropriate regulatory requirements and company manufacturing standards.

The Role

  • Analyses the results of testing and determines the acceptability of results against predetermined criteria.
  • Investigates and troubleshoots problems which occur and determines solutions or recommendations for changes and/or improvements.
  • Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation, and maintenance of the procedures, actions, and documentation necessary to ensure compliance within the operation.
  • Lead process improvement projects to improve the validation of computerized systems
  • Coordinates with other departments or outside contractors/vendors to complete validation tasks.
  • Participates in regulatory audits and communicates company’s computer validation policies.
  • Assesses company’s computer systems and identifies any potential Part 11 or Annex 11 gaps and ensure best data integrity practices are enforced.
  • Trains /advises less experienced Specialists and Technicians.
  • Advise and support all teams on computer validation activities.

The Person

  • Requires BS/BA in Engineering, Chemistry, or Life Sciences with 3+ years of related experience within the fields of computers and biotechnology.
  • Experience with process control systems necessary.
  • Possess a thorough understanding and experience of Validation Principles with good knowledge of GAMP 5, ICH Q7A, FDA parts 210 and 211.
  • Technical writing experience.
  • Experienced in the Generation of Validation documents.
  • Experience of the review and approval of Validation documents.
  • Strong attention to detail and accuracy.
  • Experience in risk assessments in relation to validation activities.

For further details please contact; Paula O’Reilly on 087 7094141 or send CV in confidence to paula.oreilly@lifescience.ie