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Technical associate

Tralee
Astellas Pharma
€35,000 - €60,000 a year
Posted: 11 October
Offer description

Description
Technical Associate - Tralee

About Astellas
At Astellas we are making treatments that matter to people.

We are tackling the toughest health challenges putting the patient at the heart of every move we make.

Our global vision for Patient Centricity is to support the development of innovative health solutions through a deep understanding of the patient experience. At Astellas, Patient Centricity isn't a buzzword - it's a guiding principle for action. We believe all staff have a role to play in creating a patient-centric culture and integrating an awareness of the patient into our everyday working practices, regardless of our role, team or division.

We have developed ground-breaking, innovative medicines in immunology, oncology and urology. Our medicines are extending and saving the lives of cancer patients, making transplantation possible and improving the quality of life for those living with conditions where needs are often overlooked.

We take a patient-focused approach, that allows us to convert brilliant early science into treatments and solutions that directly improve and save patients' lives.

From lab to clinic to patient, we focus on the most promising science, empower the best talent to pursue it, and develop life-changing solutions alongside the best partners.

The Opportunity
You will be responsible for performing preventive, predictive, and corrective maintenance on equipment and systems within an aseptic fill-finish pharmaceutical manufacturing facility, ensuring timely execution while working in classified cleanrooms (ISO 5–8) with appropriate gowning. You will ensure the reliable operation of production equipment, utilities, and facility systems to support aseptic manufacturing in full compliance with all internal policies and external regulatory, legislative, and statutory requirements.

You will take direction from the Team Lead and supports the execution of assigned duties, while also contributing value-added input to support plant operations, including involvement in projects and initiatives within manufacturing areas. Additionally, you will actively participate in the site's Operational Excellence Programme.

Key Responsibilities

* Equipment Maintenance & Troubleshooting

Perform routine, preventive, and emergency maintenance on aseptic fill-finish equipment (e.g., compounding systems, filling lines, lyophilizers, cappers, inspection/packaging equipment, washers, autoclaves). Troubleshoot mechanical, electrical, pneumatic, and control issues to minimize downtime while adhering to GMP, GDP, and safety standards.

* Facility & Utility Systems Support

Maintain and support critical utilities such as WFI, clean steam, compressed gases, HVAC, and environmental/room monitoring systems essential for aseptic operations.

* Compliance, Documentation & Data Integrity

Complete CMMS entries, maintenance logs, deviations, and documentation in compliance with cGMP and GDP. Ensure data integrity across computerized systems and participate in investigations as needed.

* Safety, Quality & Continuous Improvement

Ensure compliance with cGMP, ISO 14001, health, safety, and environmental standards. Contribute to problem-solving, equipment reliability, process improvements, and validation/engineering projects while fostering a culture of safety and teamwork.

* Projects, Change Controls & New Technologies

Support operational projects, change controls, and equipment qualification (IQ/OQ/PQ). Assist with the introduction of new products, processes, and technologies, continuously seeking efficiency and innovation.

* Training, Communication & Reporting

Complete all required training (OTJ/LMS), deliver training when needed, and engage in technical documentation updates. Provide timely feedback to the Team Lead, participate in meetings, and support effective cross-functional communication.

Education

* Level 6 qualification in Mechanical/Electrical/Automation/Industrial maintenance or equivalent required.

Preferred Experience

* Industry & Technical Experience

Experience in cGMP environments within pharmaceutical, biotech, or aseptic fill-finish manufacturing is an advantage, including familiarity with automated equipment, PLCs, HVAC, cleanroom systems, utilities, audits, and regulatory guidance.

* Skills & Competencies

Strong organisational, interpersonal, verbal, and written communication skills. Demonstrated ability to work independently or in a team, adapt to changing priorities, and contribute to a culture of continuous improvement.

* Analytical & Problem-Solving Abilities

Proven analytical thinking and problem-solving skills, with Lean Six Sigma (Yellow Belt or higher) considered an advantage.

Additional Information

* Position is based in Tralee.
* This position is 100% on-site.
* Willingness to undertake international travel to vendor sites occasionally.

What We Offer

* A challenging and diversified job in an international setting.
* Opportunity and support for continuous development.
* Inspiring work climate.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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