QA compliance specialist

This job has now expired please search on the home page to find live IT Jobs.

As Quality Compliance Specialist you will coordinate the development and maintenance of the site's quality system in compliance with all applicable regulatory requirements and ensure that products meet requirements of end users, and of regulatory authorities.Responsibilities:Coordinating the quality system, ensuring full compliance by all personnel with its requirementsCoordination of product quality review activities.Management of all technical agreements from initiation, review, approval and storage.Coordination and management of all track and trend activities to support manufacturing and QC..Auditing the quality system with other management personnel.Assisting in the investigation of and coordinating customer complaints/exceptions by ensuring implementation of effective corrective / preventive action where necessary.Measuring performance of the quality system and reporting on this at the management review meeting and during quality performance meetings e.g. SPM.Coordinating change control and Change plan activities.Monitoring quality performance and advising management personnel on major quality issues.Ensuring all plant personnel are fully aware of quality and cGMP requirements.Initiation and Completion of Quality related ER's as required.Establishing Corrective / Preventive Action system and procedures.Verification of effectiveness of corrective / preventive actions arising out of product, process and quality system non-compliance.Vendor evaluation and approval.Management of Supplier Audit Schedule.Performance of Vendor audits as required.Implementation review for Policy documents.Supporting all aspects inspection readiness including preparation activities, logistic activities, and generation of follow up responses and management of proof books.Documentation Controller Support - Control, distribution and archiving of documentation for the facility.

If you are a QA compliance specialist interested in this opportunity with one of the leading Pharmaceuticals companies in the Republic of Ireland, then please respond to this advert and I will give you a call to discuss in more detail.

Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement.To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales