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Process Engineer (Pharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
project
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:
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TL;DR
Process Engineer (Pharmaceutical Manufacturing): Supporting safe, efficient, and compliant manufacturing operations in a GMP-regulated pharmaceutical facility with an accent on process troubleshooting, validation, and continuous improvement. Focus on investigating deviations, optimizing process performance, supporting equipment qualification, and improving yield, reliability, and throughput.

Location: Onsite in Waterford, Ireland

Company

hirify.global’s Outsourced Technical Services department provides technical professionals to support long-term projects for global industry clients, including pharmaceutical manufacturing operations.

What you will do

  • Provide day-to-day technical support to manufacturing operations and monitor process performance.
  • Investigate process deviations, non-conformances, and manufacturing issues, and implement corrective and preventive actions.
  • Drive continuous improvement using Lean Manufacturing, Six Sigma, and Operational Excellence methodologies.
  • Analyze process data, identify bottlenecks, and support yield improvement, waste reduction, and throughput optimization.
  • Support process validation, process characterization, technology transfer, and new product introduction activities.
  • Collaborate with quality, validation, maintenance, and engineering teams on equipment commissioning, qualification, validation, and reliability improvements.

Requirements

  • Degree in Chemical Engineering, Process Engineering, Biotechnology, Pharmaceutical Science, or a related discipline.
  • Experience supporting manufacturing operations in pharmaceutical, biotechnology, or another regulated process industry.
  • Strong knowledge of process operations, troubleshooting, continuous improvement, GMP requirements, and pharmaceutical manufacturing processes.
  • Experience or ability to participate in FAT, SAT, IQ, OQ, and PQ activities.
  • Strong problem-solving, analytical, communication, and cross-functional collaboration skills.
  • Ability to work in a fast-paced, site-based manufacturing environment while complying with EHS requirements.

Culture & Benefits

  • Work on technically challenging pharmaceutical manufacturing projects in Ireland and internationally.
  • Opportunity for long-term assignments and career development.
  • Competitive benefits and collaboration with multidisciplinary manufacturing, quality, maintenance, and technical services teams.

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