At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self:Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self:Care for Everyone, we are the people behind the brands you trust. We are Opill(R), Compeed(R), Solpadeine(R), NiQuitin(R), ACO(R), and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to a blended:branded business to win in self:care. Description Overview This position is a 12 Month Fixed Term Contract. In this role you will support quality, system and process standards to ensure reliability and compliance with company standards and governmental and regulatory requirements such as EU GDP Directive 2013/C 343/EU, Human Medicines Regulation 2012 and EU 2001/83/EU and support the Galpharm and Omega Pharma Business entities. You will also coordinate elements of the Quality Management System, including Deviations, Change Control, CAPAs and document control for Perrigo Barnsley QA, ensuring all formal documents are evaluated, maintained, and distributed appropriately and promptly, Scope of the Role :Coordinate site quality systems including Deviation Management and CAPA. :Support Deviation investigations, working with departments as necessary to ensure cross linkage of deviations and escalate matters to appropriate Quality team members. :Support CAPA process, working with departments as necessary to ensure cross linkage with deviations and audits. :Prepare and support changes for the Change Management System for monthly Change Review Board, working with departments as necessary to ensure cross linkage of the required documents and process. :Participate in Self inspections where required, to ensure compliance to the Internal Audit Schedule. :Act as the point of contact for the business for Quality related queries. :Participate in continuous improvement initiatives that support site objectives. :Have the flexibility to take on additional tasks and responsibilities at the discretion of the Departmental Manager. Experience Required :1:3 years' experience in a GMP/GDP Quality Assurance Role, preferably in the Pharmaceutical Industry. :Good understanding of pharmaceutical GMP, regulatory documentation systems and ability to author, review and issue:controlled documentation, detailed report and investigations. :A good understanding of general pharmaceutical industry and operational knowledge of core QA systems. :Ability to maintain high quality documentation, manage data sources and interpret data for key Performance Indicators to judge the operational state of processes. :Work independently on QMS elements they are responsible : knowing when to escalate appropriately any issues. :Experience in the use of root cause analysis in the investigation and resolution of deviations, plus formulating appropriate CAPAs. :Experience in the use of standard business applications such as the Microsoft Office. :Experience using electronic documentation systems e.g., Trackwise, SAP, SharePoint. Benefits We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more aboutTotal Rewardsat Perrigo. Hybrid Working Approach We love our offices and the setting they provide for in:person collaboration and celebration. But