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3 часа назад

Scheduler – Capital Projects, Operations & CQV

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
Scheduler – Capital Projects, Operations & CQV (CAPEX/OPEX/CQV): Developing and maintaining integrated schedules for capital projects, facility operations, shutdowns, commissioning, qualification, and validation in a regulated life-sciences environment with an accent on critical-path analysis, schedule risk management, and cross-functional coordination. Focus on integrating construction, procurement, equipment turnover, GMP readiness, CQV protocols, and operational constraints into accurate forecasts and recovery plans.

Location: Onsite in Dover, New Hampshire, United States

Company

hirify.global is an employee-owned international project delivery firm supporting clients in pharmaceutical, food, biotechnology, medical technology, and mission-critical sectors.

What you will do

  • Develop, maintain, baseline, and update integrated schedules for CAPEX projects from design and procurement through construction, commissioning, qualification, and closeout.
  • Plan OPEX, facility shutdown, maintenance, equipment upgrade, and continuous-improvement activities.
  • Sequence commissioning, qualification, and validation work, including system turnover, IQ, OQ, PQ, documentation, and final GMP handover.
  • Coordinate schedules across Engineering, Manufacturing, Quality, Validation, Facilities, Automation, Maintenance, EHS, contractors, and vendors.
  • Analyze critical paths, float, milestones, progress, schedule variance, risks, resource constraints, and change impacts.
  • Prepare forecasts, recovery plans, look-ahead schedules, dashboards, milestone reports, and executive-level updates.

Requirements

  • Bachelor’s degree in Engineering, Construction Management, Project Management, or a related discipline; equivalent relevant experience may be considered.
  • Five or more years of scheduling or project-controls experience in pharmaceutical, biotechnology, medical-device, or other regulated manufacturing environments.
  • Experience supporting both capital-project delivery and operational or CQV activities.
  • Strong proficiency with Primavera P6 is preferred.
  • Experience with integrated Level 3 and Level 4 schedules, brownfield GMP projects, shutdowns, equipment installations, or operational-readiness programs is preferred.
  • Experience with system turnover, commissioning plans, qualification protocols, validation master plans, schedule risk assessments, earned-value analysis, or resource-loaded schedules is preferred.

Culture & Benefits

  • Employee-owned company with an inclusive culture focused on mutual respect and belonging.
  • Work alongside multidisciplinary project teams and client organizations.
  • Commitment to sustainability, corporate responsibility, inclusion, and diversity.
  • Reasonable accommodations are available for candidates with disabilities during the recruitment process.

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