G

QA Manufacturing Analyst

Job Description - QA Manufacturing Analyst
















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'll 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'll Bring:




  • 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



 


Qualifications:



  • Minimum of B.Sc Degree or equivalent third level education.

  • 1-2 years’ experience working in an aseptic pharmaceutical/medical devices industry.    


 


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-FD1


 



Location: Grange Castle International Business Park, Grange, Clondalkin, Co. Dublin, D22 K2R3    


 


Learn more about Grifols


 


Original job QA Manufacturing Analyst posted on GrabJobs ©. To flag any issues with this job please use the Report Job button on GrabJobs.
Share Job
Share Job

About the Company

Grifols Sa

Explore Grifols' comprehensive, innovative and patient-centric biopharma and healthcare solutions.

Read more about the company

Similar QA Manufacturing Analyst Jobs in Ireland

GrabJobs is the no1 job portal in Ireland, connecting you to thousands of jobs fast! Find the best jobs in Ireland, apply in 1 click and get a job today!

Mobile Apps

Copyright © 2026 Grabjobs Pte.Ltd. All Rights Reserved.