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5 дней назад

Interface Manager (Pharmaceutical Facilities)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Interface Manager (Pharmaceutical Facilities): Developing and leading interface management plans for large pharmaceutical capital projects with an accent on cross-functional coordination, governance, and interface risk control. Focus on managing technical, organizational, construction, commissioning, and operational interfaces, integrating critical-path activities, and ensuring GMP and regulatory compliance.

Location: Richmond, Virginia, United States

Company

hirify.global Sustainable Technology Solutions provides technology, advisory, engineering, energy transition, and asset optimization solutions across the full asset life cycle.

What you will do

  • Develop, implement, and maintain the project Interface Management Plan, including processes, tools, governance, and reporting systems.
  • Identify and manage technical, organizational, construction, commissioning, validation, quality, and operational interfaces throughout the project lifecycle.
  • Coordinate interfaces between engineering, procurement, construction management, commissioning, operations, contractors, licensors, clients, and third-party stakeholders.
  • Lead interface meetings and workshops, assign ownership, resolve issues, and track actions through closure.
  • Maintain interface registers covering risks, dependencies, constraints, decisions, milestones, and critical-path impacts.
  • Prepare KPIs, risk assessments, interface reports, and executive updates while ensuring compliance with GMP, quality systems, regulatory expectations, and company procedures.

Requirements

  • Bachelor’s degree in engineering or project management.
  • Minimum 15 years of industry experience, including at least 10 years supporting pharmaceutical, biotechnology, vaccine, sterile manufacturing, API, or advanced therapy facilities.
  • Experience delivering capital projects exceeding $500 million TIC.
  • Experience managing interfaces and communications for large multidisciplinary teams and contractors.
  • Strong knowledge of communications, governance, project controls, design management, and project delivery processes.

Nice to have

  • Experience with GMP-regulated facilities, major capital projects exceeding $1 billion TIC, PMC or Owner’s Representative work, FDA inspection support, or greenfield pharmaceutical projects.
  • PE, PMP, or ISPE certification.

Culture & Benefits

  • Full-time employment with a Zero Harm and People First culture.
  • Benefits may include a 401(k) plan with company match, medical, dental, vision, life insurance, AD&D, flexible spending, disability coverage, and paid time off.
  • Flexible work schedules may be available.
  • Professional training and career development opportunities.

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