Project Description

Deirdre Cahalan

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Deirdre Cahalan – Quality and Regulatory Affairs Professional

With over 25 years experience in various quality and regulatory roles within the pharmaceutical, API and medical device industries, Deirdre Cahalan is a versatile and fastidious quality professional. She has very strong experience as a regulatory affairs administrator, documentation reviewer and auditor in contract and full-time roles.

She is highly experienced in compiling regulatory submissions, PQR/APR and has effectively managed a number of quality systems including customer complaints and failure investigation. She is a qualified lead assessor.

Skills and Experience:

  • Audit and review of batch and quality documentation and specifications
  • Compilation of PQRs/APRs and Annual Reports
  • Liaising with regulatory agencies
  • Complaint and Failure Investigation Quality System management
  • Internal and vendor quality auditing. Assisting with 3rd Party quality audits
  • Managing Plant Master Files and Dossiers
  • Excellent computer skills

Information

LOCATION

Based in North Tipperary and available to work in the Clare, Limerick, Galway, Tipperary and Cork areas.

AVAILABILITY

Available August 2019.