Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль описана понятно и охватывает полный цикл проектов в фармацевтическом производстве, но работа через подрядчика может ограничить долгосрочную стабильность на одном объекте.
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Текст:
Hirify AI/Оригинал
TL;DR
Project Engineer (GMP Manufacturing / Utilities): Delivering strategic capital projects for a pharmaceutical manufacturing facility from concept and design through commissioning, qualification, and handover with an accent on GMP clean utilities, project controls, and regulatory compliance. Focus on managing cross-functional teams, contractors, budgets, risks, and technical documentation across highly automated production projects.
Location: Hybrid — Dublin, Ireland
Company
hirify.global is an employee-owned international project delivery firm serving pharmaceutical, food, medtech, and mission-critical sectors through offices in Europe, Asia, and the US.
What you will do
Support and deliver capital projects across the full lifecycle, from concept and design through commissioning, qualification, handover, and closeout.
Lead or support cross-functional teams delivering manufacturing, process, facility, and utility projects in a highly automated GMP environment.
Provide technical expertise in utilities, ideally GMP clean utilities, acting as a System Owner or Project Engineer where required.
Ensure compliance with safety requirements, engineering standards, GMP, EHS expectations, and regulatory requirements.
Build stakeholder relationships and support project documentation, operating procedures, maintenance strategies, and handovers.
Requirements
Degree, preferably Level 8, in Engineering, Science, or a related discipline.
5+ years of experience as a Project Engineer in a GMP manufacturing environment.
Experience delivering facility, process, and utility projects, including clean utility systems, with technical knowledge as a System Owner or Project Engineer.
Strong understanding of the full project lifecycle, including design, implementation, commissioning and qualification, and handover.
Proven ability to manage projects from initiation to completion and deliver on schedule.
Experience coordinating cross-functional teams and external contractors.
Excellent communication, organisation, and stakeholder management skills.
Experience delivering documentation and project handovers right first time.
Ability to develop operating procedures and maintenance/calibration strategies with end users.
Proficiency in Microsoft Office applications and strong understanding of GMP principles and EHS requirements in pharmaceutical manufacturing.
Culture & Benefits
Employee-owned company with an inclusive culture based on mutual respect, belonging, and diversity.
Commitment to corporate responsibility and sustainability through the 2025 business strategy.
Fair and accessible hiring process with reasonable accommodations for candidates with disabilities.
Applications are treated in the strictest confidence.
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