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QA Manufacturing Analyst
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
6d

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QA Manufacturing Analyst

Grifols Worldwide Op Ltd -
Dublin, County Dublin

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Job details

Full-time
6 days ago

Benefits

Private medical insurance

Qualifications

Bachelor's degree
Organisational skills
Communication skills

Full job description

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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

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