Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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У роли понятная зона ответственности, крупный масштаб проектов и профильные требования к фармацевтическому опыту, но без диапазона зарплаты сложно оценить условия относительно рынка.
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Зарплата не указанаПонятная рольКрупные проектыФармацевтическая экспертиза
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Project Management Office Manager (Pharmaceutical): Leading governance, reporting, project controls, and integrated planning for large pharmaceutical capital projects with an accent on stage-gate reviews, executive dashboards, risk management, and GMP compliance. Focus on consolidating multidisciplinary project performance, managing scope and schedule changes, and coordinating engineering, procurement, construction, commissioning, and operational readiness activities.
Location: Richmond, Virginia, United States
Company
hirify.global Sustainable Technology Solutions provides lifecycle solutions covering licensed process technologies, advisory services, technical expertise, energy transition, design, and asset optimization.
What you will do
Develop and maintain the PMO framework, including governance processes, procedures, standards, templates, and reporting requirements.
Lead stage-gate reviews, executive reviews, decision management, action tracking, governance audits, and compliance activities.
Prepare executive dashboards, KPI reports, project status presentations, and integrated governance packages for senior leadership, clients, and steering committees.
Coordinate project controls, integrated planning, document control, meeting management, and reporting across engineering, procurement, construction, commissioning, validation, and operational readiness teams.
Manage and mentor PMO, project controls, planning, cost engineering, and reporting personnel while driving continuous improvement.
Requirements
Bachelor’s degree in Engineering, Construction Management, Business, Project Management, or a related discipline.
At least 10 years of project management experience and 5 years supporting pharmaceutical, biotechnology, vaccine, sterile manufacturing, API, or advanced therapy facilities.
Experience with capital projects exceeding $500 million TIC and large multidisciplinary teams and contractors.
Strong knowledge of communications, governance, project controls, design management, and project delivery processes.
Knowledge of pharmaceutical regulations, GMP requirements, quality management systems, company procedures, and contractual obligations is required for applicable project delivery.
Nice to have
Experience supporting GMP-regulated facilities or greenfield pharmaceutical projects.
Owner’s Representative or PMC experience on major capital projects exceeding $500 million TIC.
PE, PMP, or ISPE certification.
FDA inspection support experience.
Culture & Benefits
401(k) plan with company match and medical, dental, vision, life, AD&D, flexible spending, and disability benefits.
Paid time off and a flexible work schedule.
Professional training and career development opportunities.
People First culture focused on belonging, connection, growth, teamwork, and Zero Harm.
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