Quality Analyst - NEW**

Quality Analyst opportunity with a Global Pharmaceutical company in Dublin.

The main function of this role is to support Quality Operations.

Key responsiblilities:
•    Management and maintenance of the Quality documentation system.
•    Issuance and tracking of change controls, deviations, CAPAs, complaints, etc.
•    Life-cycle management of SOPs, Forms and other related documents for all departments.
•    Have the capacity to train personnel on salient aspects of the Quality System, e.g., for SOP updates, and mentor and instruct others on the correct use of it.
•    Be the main point of contact for personnel for documentation/systems related matters.
•    Be involved in the development and implementation of different aspects of the Quality System that will be rolled out across the company.
•    Assist in the development and execution of annual GMP training.
•    Assist in the development and presentation of Quality metrics to Corporate.
•    Adherence to Company Health & Safety procedures
•    Participate in training programmes

Key Requirements:
Bachelor’s degree in science is required

•    Minimum 3 years Pharmaceutical experience preferable with a global pharmaceutical organisation, experience should be in quality assurance, quality control or manufacturing
•    A thorough understanding of Quality Systems and cGMP’s
•    Experience with and a fundamental understanding of European GMP’s
•    Proven communication skills. Exposure to International Pharmaceutical Practices and Requirements.

For full job spec and details email Tina at tdunne@thornshaw.com or call +01 2784671
www.thornshaw.com        Thornshaw Scientific is a CPL group company.