QA Manufacturing Analyst

Grifols, S.A; Dublin; On-site; EUR 55,000 - 70,000; Full time

Benefits offered by this job

Highly competitive salary

Annual performance based bonus

Shares options scheme

Group pension scheme

Private Medical Insurance for the员工

Job summary

Grifols, S.A. is seeking a QA Manufacturing Analyst for a new purification and aseptic filling plant at Grifols Worldwide Operations (GWWO).

The role reports to the Quality Assurance Monitoring Supervisor and focuses on aseptic sampling and environmental monitoring to establish the monitoring programme for aseptic manufacture and water systems. The position requires a B.Sc degree or equivalent and 1–2 years in aseptic pharma, with strong communication and organizational skills and a proactive

Qualifications

• Minimum of B.Sc Degree or equivalent third level education.
• 1-2 years’ experience in 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.

Responsibilities

• Support the Quality Monitoring Supervisor and act as delegate when required.
• Collaborate with cross-functional teams to deliver monitoring activities and share quality insights.
• Perform 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.

Skills

Communication

Organisational skills

Proactive mindset

Flexible approach

Education

B.Sc Degree or equivalent

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 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
• Wellness activities - Social activities eg. Padel, Summer Events