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QC Analyst Technical Writer

  • Sector: Science & Pharma
  • Contact Email:
  • Job Ref: 19594

We are working in partnership with our client based in Dublin. We have an opening for a Quality Control Technical Writer to join an established and leading Global Pharmaceutical Company based in Athlone.

This is a Fixed Term Role within the QC Laboratory Services. Reporting to the QC Laboratory Supervisor the successful for supporting the work of the QC group in accordance with GMP.


Job Responsibilities:

  • Lead QC Technical documentation projects as an individual contributor.
  • Accountable for timely completion of projects within the technical writing role.
  • Collaborate with internal resources and business partners to support project requirements and ensure project completion.
  • Work in accordance with cGMP and GLP requirements.
  • Ensure consistent and good documentation practices are followed.
  • Creation, review, and update of documentation, e.g. Laboratory Technical Protocols and Reports, Standard Operating Procedures, and Analytical Protocols.
  • Translating complex topics into clear, concise, and understandable topics is required.
  • Review standards for documentation types, structure, and assembly so that content is organised logically with the end reader in mind.
  • Maintain Documents in the document management system.


Job Requirements:

  • Third Level Qualification (BSc or Higher) in Science-related Discipline.
  • Minimum of 3 Years of Experience within a Technical Writer role in a GMP/Pharmaceutical/Quality Environment.
  • Excellent Communication and report writing skills.
  • Proficient in the use of MS Office Suite.
  • Experience in deviation and investigation writing.
  • Disciplined, deadline-driven, and focused Right First Time.
  • Experience using Quality documentation management systems. 

If you would like more information on this role you can contact Paul Dunican

(090) 641 7022