Our client, a growing Dublin based biopharmaceutical company, are currently recruiting for a Quality Assurance Associate.
Main Duties / Responsibilities: 1) Manage the Documentation Control process 2) Prepare policies and procedures 3) Co-ordinate the implementation of the Internal and external audit schedules and ensure the timely completion of audits 4) Oversee the effective documentation and tracking of QMS activities, including deviations and change controls, and the implementation of corrective actions 5) Lead the vendor oversight process, including analysis of Key Performance Indicators (KPIs) 6) Review GMP and GCP documentation as required, such as batch records, technical reports and clinical trial protocols 7) Conduct audits of vendors and contractors when required 8) Generate and maintain Technical Agreements with suppliers and customers in line with relevant regulatory and business requirements 9) Ensure that all activities are in compliance with the requirements of Good Manufacturing Practice and Good Clinical Practice. 10) Contribute to Company Training procedures as required 11) Carry out various other additional tasks that may be required from time to time in accordance with the overall goals of the company
Requirements: 1) Scientific degree 2) 3+ years of relevant GMP experience in the pharmaceutical industry, 3) QA auditing experience 4) Knowledge of relevant regulatory requirements 5) Strong computer skills 6) Ability to travel as required 7) Excellent communication skills
For more information and to apply for this role please call Linda on 1 or e-mail
Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. Tel: 1