Quality Systems Specialist

Working with my client on a new role for a Quality Systems Specialist. Permanent opportunity with a global pharmaceutical company.

Key responsibilities and reporting to the QA Compliance Manager:

· Support the ongoing management of electronic Quality Management Systems (eQMS) related, but not limited to the following processes: Documentation management, Change controls, Deviation management, CAPAs, Customers complaints and Laboratory Investigations.

· Lead and execute development and /or modification of the company's eQMS.

· Develop and approve any written procedures and other documents including amendments to those documents (e.g. SOP's WISOP's Technical agreements, Quality Policy and other compliance related documents.) required in support of eQMS.

· Develop and maintain dashboard reports ensuring accurate, complete, and consistent data is available providing meaningful trending and analysis of data across all quality systems.

· Participate in the preparation of and delivery of associated training on site.

· To collaborate with the corporate Quality Systems Specialist to contribute to the development maintenance of the quality systems.

· Work collaboratively with all site departments to ensure high levels of GMP.

· Participate in the preparation of and follow up of regulatory and other external inspections of SII

Position Requirements

Essential:

3+ years' experience in the Pharmaceutical Industry and a 3rd level qualification in a scientific discipline.Strong communication skills and interpersonal skillsStrong IT skillsStrong writing skillsStrong attention to detail

For more information and to apply for this role please call Tina or Zoe on or e-mail or

Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. Tel:

#LI-TD1

---