QA Validation specialist

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The QA Validation specialist, based in Dublin, executes the site QA activities in order to protect the safety, quality and efficacy of products, thereby ensuring the availability of correct, safe product for the Patients, and assuring the security of the company's business and global markets. This key role must ensure effective interaction with other departments and locations regarding GMP Document review and finished product releases. In particular, this will involve partnering with major stakeholders such as Operations, QC, Facilities, Engineering and Supply Chain to optimise patient supply. Role responsibilities:Provide quality and cGMP input and oversight for all start-up project activities through commercial readiness and ongoing product disposition.Provide QA support for risk based verification activities in the capacity of Quality Assurance Subject Matter Expert. Review and approval equipment/utilities verification documentation from design to post execution.Participate in verification quality risk assessments and provide quality oversight to ensure verification quality risk assessments are effectively maintained/controlled.QA support for implementation of Manufacturing Execution System (MES) computer system validation deliverables.Review and approval of engineering functional area documentation (SOP, Work Instructions, Criticality Assessments, technical report and protocols).Authoring, review and approval of QA-related procedures.Oversee the effective documentation and tracking of quality management system activities including deviations and change controls and CAPA.Review and approve Validation protocols as required. (Examples include cleaning, process, method validation). Support the vendor quality management programme.Participate in regulatory inspections as required.Develop and report quality metrics.Provide quality oversight of calibration and preventative maintenance criticality assessments as required.Represents Quality Assurance to guide various projects and technical meetings, as needed.Responsible for documenting and reporting compliance issues to management.Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements.Any other duties as expressed by the manager.Qualifications:Min 5 years QA experience in a pharmaceutical manufacture/bio pharmaceuticals environment. (BDS experience is essential).Must have strong process knowledge to include upstream and/or downstream processing.An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment.Excellent communication & presentation skills are essential.Excellent time management organizational skills along with a proven ability to multi-task.If you are interested in this role and would like to learn more, please respond to this advert, and I will call you to discuss in more detail. *Please note, in order to be eligible for this role you must hold a valid EU passport, or a stamp 4/1G visa*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