8 дней назад
Calibration/Steam Sterilisation Qualification Specialist
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Calibration/Steam Sterilisation Qualification Specialist (Calibration, Sterilisation and Quality): Maintaining and qualifying calibration and sterilisation processes in a regulated manufacturing environment with an accent on equipment reliability, GMP compliance, and patient safety. Focus on performing instrument calibration, leading installation, operational, and performance qualification studies, reviewing sterilisation cycles, and resolving process deviations.
Location: Castlebar, Mayo, Ireland
Company
develops vital organ therapies and digital solutions, with a focus on improving kidney care, dialysis, and patient outcomes.
What you will do
- Perform calibration, maintenance, verification, troubleshooting, adjustment, and repair of measurement and test equipment.
- Coordinate external calibration and recertification activities, including documentation review and instrument inspections.
- Manage calibration scheduling, tracking systems, and accurate compliance records.
- Lead and support steriliser qualification activities covering installation, operational, and performance qualification studies.
- Review and approve sterilisation cycles and related documentation, and support sterility assurance activities involving deviations and non-conformances.
- Collaborate with Quality, Engineering, Operations, and Maintenance teams during audits, regulatory inspections, and continuous improvement initiatives.
Requirements
- 2–4 years of experience in calibration, sterilisation, validation, engineering, maintenance, or quality within a regulated manufacturing environment.
- Technical qualification in Engineering, Science, Quality, Manufacturing, or a related discipline preferred.
- Strong technical aptitude, analytical and problem-solving skills, attention to detail, and commitment to quality and compliance.
- Ability to communicate and collaborate effectively across functions.
- Experience in GMP-regulated environments is desirable.
- Proficiency in Microsoft Office and experience with calibration management systems are desirable.
Culture & Benefits
- Safety-focused work environment guided by Environmental, Health & Safety policies and regulatory requirements.
- Cross-functional collaboration across Quality, Engineering, Operations, and Maintenance.
- Work focused on product quality, compliance, operational efficiency, and patient safety.
- Reasonable accommodations are available for candidates with disabilities during the application and interview process.
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