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Grifols

Dublin QA Manufacturing Analyst

Grifols · 545135

Full-timeOn-sitePosted 21 October 2026
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Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment. Position Summary: The QA Manufacturing Analyst is required for a new purification and aseptic filling plant for the blood protein albumin at Grifols Worldwide Operations (GWWO). Reporting directly to the Quality Assurance Monitoring Supervisor of GWWO, the role is for an experienced analyst who will perform aseptic sampling and environmental monitoring as part in the establishment of the Environmental Monitoring programme for aseptic manufacture and water systems for the manufacturing operations at GWWO. What You Will Do: Support the Quality Monitoring Supervisor and act as delegate when required Collaborate with cross-functional teams to deliver monitoring activities and share quality insightsPerform environmental and water sampling, supporting cleanroom and sterilisation qualifications Contribute to investigations (deviations, CAPA, change controls) and provide QA support to manufacturing Support audits, inspections, product quality reviews, and GMP compliance across the site Assist with training, continuous improvement, and implementation of best practices Participate in validation activities, including media fills and process validation Support additional quality activities as needed What You Will Bring: Minimum of B.Sc Degree or equivalent third level education. 1-2 years’ experience working in an aseptic pharmaceutical/medical devices industry. Solid understanding of aseptic regulatory requirements. Experience in Grade C/D environments, with exposure to Grade A/B an advantage. Experience in cleanroom environmental monitoring within aseptic pharma or medical device setting. Strong communication and organisational skills, with a proactive and flexible approach. Our Benefits Include: Highly competitive salary Annual performance based bonus % Shares options scheme Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match Private Medical Insurance for the employee Ongoing opportunities for career development in a rapidly expanding work environment Succession planning and internal promotions Education allowance Wellness activities - Social activities eg. Padel, Summer Events We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you #LI-AM1 Location: Grange Castle International Business Park, Grange, Co. Dublin, D22 K2R3 Learn more about Grifols Apply now » Find similar jobs: EMEA, all_jobs, ALLJOBS/, ALLJOBS Grifols LinkedIn Privacy Notice Cookies Policy Cookies Settings Additional Candidate Resources © 2026 Grifols, S.A. All rights reserved worldwide Cookie Consent Manager When you visit any website, it may store or retrieve information on your browser, mostly in the form of cookies. Because we respect your right to privacy, you can choose not to allow some types of cookies. However, blocking some types of cookies may impact your experience of the site and the services we are able to offer. Strictly Necessary Cookies These cookies are necessary for the website to function and cannot be switched off in our systems. They are usually only set in response to actions made by you which amount to a request for services, such as setting your privacy preferences, logging in or filling in forms. 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