Who we areUniphar Group is a rapidly expanding diversified healthcare services business with a global footprint and a proud heritage in Ireland. Since Uniphar became a publicly listed company in 2019, the Group has grown organically and through a series of strategic acquisitions, which continue to strengthen Uniphar’s international reach. Uniphar provides outsourced and specialised services to its clients, leveraging the strong relationships with 200+ of the world’s best known pharmaco-medical manufacturers across multiple geographies, enabled by our cutting-edge digital technology and our expert teams. Uniphar is organised into three key divisions: Supply Chain & Retail, Commercial & Clinical (Med Tech / Pharma) and Product Access.With a workforce of close to 3,500 spread across Ireland, United Kingdom, the Netherlands, the Nordics, Germany and the USA, Uniphar is a trusted global partner to Pharma and MedTech manufacturers, working to improve patient access to medicines and treatments around the world.Culture at UnipharWe pride ourselves in being truly entrepreneurial, innovative, collaborative, with a strong problem-solving ethos. We have built working relationships which span decades with many of the world’s largest Pharma and MedTech companies. We believe that this is because we know how to build a relationship of trust with our partners - we put our customers and their patients at the heart of what we do and treat them with integrity and respect. Everything Uniphar does is enabled by our people. As we continue to grow domestically and internationally, we become more diverse. This rich diversity fuels our business and enriches our culture.The role - This is a fixed term one year contract.The purpose of this role will be to work within a cross functional environment to foster an ethos and culture of cGxP & quality awareness & to ensure compliance with the requirement of ISO 9001, regulatory and principal requirements.Be the direct point of contact for all company, quality related matters.Support the day-to-day activities of the Pharmacovigilance (PV) Coordinator & engage in PV activities, as required.Participate in Quality Management System harmonisation activities.Ensure the highest quality, compliance, and safety standards.Represent Quality in support of Deviations, Risk Assessments, Change Controls & CAPAS including active participation in investigations and problem resolution.Provide overall quality direction and oversight for key functional areas/departments, ensuring that programs, policies, and procedures are robust and in keeping with regulatory, internal & client expectations.Update, review & approve Standard Operating Procedures, Work Instructions and Quality related documentation, as required.Implement the necessary customer & supplier Bona Fide checks.Lead & coordinate quality system audits & schedules - internal, external & MAH.Establish, develop & implement Technical/Quality Agreements, as .Participate in customer complaint investigations.Be an active member of the company's Clinical Governance (CG) committee, ensuring the compilation & presentation of the relevant CG activity reports.Prepare weekly, monthly, quarterly & annual reports and/or reviews, as required.Lead coordinate & engage in rework activity.Lead coordinate & participate in all ISO required activity to ensure continuous maintenance of the company's ISO Standard.Develop and undertake induction and routine quality training of new and current employees.Perform any other related duties as assigned from time to time based on company needs.#unipharsupplychain&retail