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Process Mechanical Engineering Manager (Pharmaceutical)

Формат работы
hybrid
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
Process Mechanical Engineering Manager (Pharmaceutical): Leading process mechanical engineering projects for pharmaceutical, biotechnology, and cell and gene therapy manufacturing facilities with an accent on process systems, GMP utilities, piping, equipment integration, and multidisciplinary delivery. Focus on managing engineering teams, approving technical deliverables, coordinating vendors and project disciplines, and supporting commissioning, qualification, and startup.

Location: Hybrid role based in Conshohocken, Pennsylvania, supporting the Philadelphia area team. Periodic travel is required for project execution and client engagements.

Company

hirify.global is an employee-owned international project delivery firm with more than 4,000 employees serving pharmaceutical, food, biotech, medical technology, and mission-critical sectors.

What you will do

  • Lead, mentor, and develop the Process Mechanical Engineering team, including resource planning, recruitment support, performance management, and career development.
  • Lead multidisciplinary engineering projects from feasibility and conceptual design through detailed design, construction documentation, procurement, commissioning, and startup.
  • Manage project scope, schedules, staffing, quality, budgets, technical performance, and commercial delivery.
  • Develop, review, and approve equipment lists, cost estimates, technical specifications, basis of design documents, layouts, procurement packages, calculations, and reports.
  • Coordinate clients, vendors, contractors, and internal process, piping, electrical, automation, instrumentation, architectural, and CQV disciplines.
  • Drive technical problem-solving, risk identification, constructability reviews, equipment package development, and compliance with GMP, codes, standards, and QMS requirements.

Requirements

  • Bachelor's degree in Mechanical Engineering, Chemical Engineering, Process Engineering, or a related discipline.
  • 12+ years of engineering design experience in consulting, EPCM, or engineering services.
  • Experience with pharmaceutical, biopharmaceutical, biotechnology, cell and gene therapy, or other regulated life sciences facilities.
  • Demonstrated experience leading multidisciplinary engineering projects and managing project teams.
  • Strong knowledge of process systems, process and GMP utilities, process equipment integration, piping systems and specifications, GMP facility design, and engineering documentation.
  • Experience with project planning, budgeting, resource management, client communication, industry codes, regulatory requirements, and periodic project-related travel.

Nice to have

  • Experience in EPCM project delivery environments.
  • Familiarity with Navisworks, 3D design coordination, and advanced engineering design tools.
  • Experience leading teams across multiple offices and project locations.

Culture & Benefits

  • Employee-owned organization focused on people, clients, trade partners, sustainability, and corporate responsibility.
  • Inclusive workplace committed to mutual respect, belonging, and diversity.
  • Fair and accessible hiring process with reasonable accommodations available for candidates with disabilities.

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