Our client organisation are globally renowned within the medical device sector, producing deliverable devices for leading companies within the pharmaceutical and primary healthcare sectors. The company employ 560 individuals in Ireland and are expanding rapidly, helping pharmaceutical companies to deliver for their customers and to help patients worldwide. Due to this expansion, the organisation are looking to add a Validation Engineer to their team. The Role: As the Validation Engineer you will be working within a team and will frequently be in contact with the Site Quality Manager as well as the Senior Validation Engineers. The Validation Engineer develops and implements validation and qualification policies, procedures and protocols. Additionally, you will be required to; Review and analyse protocol data to determine if requirements are met. Prepare and submit protocol reports for internal and customer review. Recommend corrective action where necessary and develops matter validation plans. The Person: The successful Validation Engineer will have: 2-4 years previous experience in a Validation position in healthcare or another highly regulated field. A BSc in Engineering or a related discipline. Experience developing and executing validations through all phases and a knowledge of 21 CFR 820, or 21 CFR 210, 211 and Part 11, a plus is beneficial. A working knowledge of ISO 13485 and GMP standards is also beneficial. This position offers an excellent remuneration package and may require travel as per the requirements of the project. To discover more about this opportunity, apply now or contact Conor Britchfield at HRM on 353 1 632 18 70 for a confidential discussion. This job originally appeared on RecruitIreland.com.
Position: Validation Engineer, Dublin
70 days ago