Cache of job #13850466


FRS Recruitment

Job Title

QA Specialist


My client is a global pharmaceutical company focused on developing and delivering products to improve people's lives. Due to expansion and ongoing projects they are have a fantastic opportunity for 2 x QA Specialists to join their team based in Cork. What's in it for you? This is a superb opportunity to work in a Quality Assurance environment for a global pharma giant that serve patients with life-improving treatments. Working here will be a fantastic addition to your CV. Your work will truly make a difference to people's lives and you will work alongside cutting-edge technology and a supportive and friendly team. There is a lucrative 12 contract on offer. General Responsibilities: Working in the QA team you'll be involved with: - Carrying out tasks and projects related to compliance activities during qualification and validation related to projects as required by Good Manufacturing Practice (GMP. - Review and approval of change controls, non-conformance investigations, and protocols. - Support and direct all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met following the Standard of Leadership behaviour model. - Batch Record Review & material release to ensure compliance with GMP requirements. - Administration of event management systems including Review & Approval of Event, Deviations, and Customer complaints. - Management of batch records design and approval. - Administration of the SAP Quality Management Module. - Management of site change control systems. - Annual Product Reviews. - Supporting validation activities on site as described in the Site Validation Master Plan. - Reviewing SOPs/work instructions/forms from other departments on behalf of Quality Assurance. - Assist with the preparation for regulatory and customer GMP inspections of the site. - Participate in the introduction of new process or modified process steps, as part of a New Product Introduction Team (NPI. - Performing GMP audits on-site and vendor facilities as required. The Fit: The ideal candidate will have a Third Level qualification in Science/Pharma with 2 years industry experience in a QA position. Next Step: APPLY NOW. No updated CV or have some questions before applying? Call Leo for a confidential chat on 086 049 5443 or connect with me on: LinkedIn at or Twitter: This job originally appeared on



Date Added

103 days ago