5 Monitoring Analyst jobs in Ireland

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:

QA Environmental Monitoring 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 Grifols Worldwide Operations (GWWO).

This role offers a chance to work in a state-of-the-art facility, in an innovative Biotechnology company with excellent career development opportunities and a clear and committed patient focus.

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.

KEY RESPONSIBILITIES:

Act as a delegate for the quality environmental supervisor when required.

Communication:

• Liaise with Validation, Quality Control, Quality Manufacturing Assurance, Maintenance and the Operations team on execution of monitoring protocols.
• Provide quality performance information as required
• Ensure regular Quality interaction with other Departments

Quality Assurance Activities:

• Reviewing and support sampling plans for water systems.
• Routine sampling of Purified Water and Water for Injection.
• Assist and participate in qualification of clean rooms and sterilisation processes, aseptic gowning and other qualification processes where required.
• Lead and/participate in Environmental excursion investigations, deviations, CAPA and change controls and provide Quality support to the manufacturing area.
• Support the spot check/walk-through process of the lines.
• Support the annual product quality reviews if required.
• Training of new Quality personnel where appropriate.
• GMP implementation and site-wide Quality Awareness.
• Liaise with other Department representatives to promote improvements in GMP and Quality standards.
• Leading and implementing innovation, best practices and solutions for drug product manufacturing in collaboration with Quality teams from the Grifols sister sites.
• To support sampling plans for Media Fill and Process Validation batches.
• To support any other additional activities as assigned by the QA manufacturing Monitoring Supervisor or the QA Manufacturing Manager

PERSON SPECIFICATION

• Excellent communication skills
• Self-motivated
• Good organizational skills
• Flexibility
• Cleanroom performing Environmental Monitoring within the aseptic pharmaceutical/medical devices industry.
• Deep knowledge and understanding of the aseptic regulatory requirements
• Minimum of B.Sc Degree or equivalent third level education and at least 2 years' experience working in an aseptic pharmaceutical/ medical devices industry.
• Grade C/D environmental monitoring experience.
• Possibility of Grade A/B environmental monitoring experience.

Our Benefits Include:

• Highly competitive salary
• Group pension scheme - Contribution rates are (1.5% / 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

Learn more about Grifols

About the Company

My client are a leading provider of professional scientific services, supporting world-class biopharmaceutical and biotechnology facilities. Their mission is to deliver high-quality laboratory and environmental monitoring services while fostering innovation, compliance, and collaboration. They believe in empowering their teams with career development, training, and the opportunity to work in cutting-edge facilities.

About the Position

We are seeking a detail-oriented Microbiology & Environmental Monitoring Analyst to join a team in Limerick. In this role, you will perform cleanroom and utility monitoring, microbiological sampling, and analysis in compliance with GMP standards. This is a key position supporting the manufacture of life-saving products in a state-of-the-art facility.

Key Responsibilities

• Perform environmental monitoring in cleanroom and manufacturing areas (ISO 8).
• Carry out viable and non-viable monitoring of air, surfaces, compressed gases, and utilities.
• Conduct sampling and testing of water systems, ethanol points, and clean steam.
• Support investigations by performing ad-hoc sampling and swabbing as required.
• Maintain strict aseptic technique, gowning, and cleanroom behaviours.
• Accurately document all results in line with GMP and data integrity standards.
• Report and investigate anomalies, contributing to continuous improvement initiatives.
• Support shutdown and response monitoring activities to enable manufacturing readiness.
• Collaborate with colleagues to deliver a robust and compliant environmental monitoring programme.

Experience/Requirements

• Bachelor's degree in Microbiology, Biochemistry, or a related life science discipline.
• Experience working in a cleanroom or microbiology laboratory environment is an advantage.
• Knowledge of GMP requirements and aseptic techniques.
• Strong attention to detail, with excellent documentation and data recording skills.
• Ability to work effectively in a collaborative, team-oriented environment.
• Flexibility to work a shift pattern (07:00 – 19:00).
• Strong problem-solving and analytical skills.
• Commitment to quality, safety, and continuous learning.