Quality Specialist

Our client, a leading global healthcare company based in Sligo, is seeking to hire a Quality Specialist on an initial eight-month contract.The successful individual will conduct quality-related activities such as preparing compliant documents & records; review & approval of quality records, product labels and product specification documents; and will help to support implementation of projects within a global Supplier Quality Organisation.Responsibilities (Full job description available on request):Contributes to and ensures timely achievement of overall project goals and tasks. Independently manages daily work schedule to perform assigned duties that support project goals.Ensures compliance to global policies and procedures through creation of compliant records and documentation.Has a right-the-first time focus and an eye for detail to ensure records generated and reviewed are accurate. Review multiple data sources and records at the same time, to identify GAPs and follow leads to investigate solutions. Helps to provide GAP analysis, data sets and justifications in support of change. Uses global and local network to execute changes.Ensure that assigned projects and tasks are performed to meet the quality requirements of customers, internal quality systems, internal & external auditors and other external agencies.Recording and analysis of metrics and trends for key supplier quality processes.Ideal background:Bachelor’s degree in Life Science, Pharmaceutical Science, Quality or closely related discipline OR relevant combination of education and experience.1-2 years’ experience working in Quality or a related field in commercial cGMP health care facility. Less experience may be appropriate with advanced degree.Experience with Microsoft Word and Excel and having an eye for detail is essential.Takes initiative and follows through with others to ensure tasks get completed on time. Ability to work independently, with colleagues and with minimal management oversight.