QA Manufacturing Analyst

Grifols

Dublin

Sur place

EUR 50 000 - 70 000

Plein temps

Il y a 2 jours
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Avantages offerts par ce poste

Annual bonus
Shares options scheme
Group pension scheme
Private medical insurance
Education allowance
Wellness activities

Résumé du poste

Grifols is seeking a QA Manufacturing Analyst for a new purification and aseptic filling plant in Grange, Co. Dublin. You will perform aseptic sampling, environmental monitoring and support the Environmental Monitoring programme for aseptic manufacture and water systems.

Ideal candidates have a B.Sc or equivalent and 1–2 years in aseptic pharma/medical devices, with strong regulatory knowledge and communication skills. The role offers a competitive package and career growth within Grifols.

Qualifications

  • Experience in aseptic pharmaceutical/medical devices industry.
  • Solid understanding of aseptic regulatory requirements.
  • Strong communication and organisational skills.
  • Experience working in Grade C/D environments is preferred.

Responsabilités

  • Support the Quality Monitoring Supervisor and act as delegate when required.
  • Collaborate with cross-functional teams to deliver monitoring activities and QA insights.
  • Perform environmental and water sampling for cleanrooms 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.

Connaissances

Aseptic environment
Regulatory knowledge
Communication skills
Organizational skills
Proactive attitude

Formation

B.Sc or equivalent

Description du poste

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

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

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