Назад
Company hidden
5 дней назад

Reliability Engineer (Pharmaceutical Manufacturing)

54 800 - 73 067
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Ireland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Reliability Engineer (Pharmaceutical Manufacturing): Improving the reliability and performance of Fill and Finish production equipment with an accent on predictive maintenance, equipment analysis, and GMP-compliant engineering support. Focus on conducting RCA and FMEA, optimizing maintenance strategies, analyzing MTBF and MTTR data, and solving chronic equipment reliability issues.

Location: Waterford, Ireland; standard day shift

Salary: €54,800–€73,067 per year

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines.

What you will do

  • Lead reliability improvement initiatives for Fill and Finish equipment, including filling lines, lyophilizers, and ancillary systems.
  • Develop predictive, preventive, and condition-based maintenance strategies to improve uptime and OEE.
  • Provide troubleshooting and technical support to production, maintenance, quality, and engineering teams.
  • Conduct RCA, FMEA, and reliability analyses for equipment failures and chronic issues.
  • Analyze MTBF, MTTR, availability, and other reliability KPIs to drive continuous improvement.
  • Support qualification, validation, deviations, CAPAs, change controls, audits, and GMP-compliant documentation.

Requirements

  • Bachelor’s degree in Mechanical, Electrical, Industrial, or related Engineering.
  • Significant experience in reliability engineering, preferably in pharmaceutical or sterile manufacturing.
  • Strong knowledge of reliability engineering methods including RCA, FMEA, and RCM.
  • Experience with data analysis, statistical methods, CMMS, and predictive maintenance technologies such as vibration analysis, thermography, or oil analysis.
  • Understanding of GMP and pharmaceutical manufacturing standards, with experience supporting compliant qualification and validation activities.
  • Strong analytical, problem-solving, project management, communication, and cross-functional collaboration skills.

Nice to have

  • Experience with Fill and Finish operations or aseptic processing.
  • Microsoft Office and data visualization experience.
  • Lean Six Sigma Green Belt or higher certification.

Culture & Benefits

  • Work in Manufacturing & Supply to support the delivery of life-changing treatments.
  • Opportunities to develop skills and explore cross-functional roles.
  • Support a global product pipeline with more than 30 planned launches by 2030.
  • Access to company employee benefit programs, subject to eligibility.
  • Work in an environment focused on growth, discovery, inclusion, and equal opportunity.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →