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Scheduler – Capital Projects, Operations & CQV

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Singapore/US/Ireland
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 and CQV): Developing and maintaining integrated schedules for capital projects, facility operations, commissioning, qualification, and validation activities in a regulated life-sciences environment with an accent on critical-path analysis, schedule risk management, and cross-functional coordination. Focus on integrating engineering, procurement, construction, shutdown, equipment, and CQV activities while building forecasts, recovery plans, and execution reports for complex GMP initiatives.

Location: Onsite near Dover, New Hampshire, United States

Company

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

What you will do

  • Develop, maintain, and update integrated schedules for CAPEX projects from design and procurement through construction, commissioning, qualification, and closeout.
  • Plan OPEX, facility shutdown, maintenance, equipment implementation, and continuous-improvement activities.
  • Sequence commissioning, qualification, and validation activities, including turnover, system completion, IQ, OQ, PQ, and final handover.
  • Analyze critical paths, float, milestones, progress, schedule variance, risks, resource constraints, and recovery options.
  • Coordinate schedules with engineering, construction, manufacturing, quality, validation, facilities, automation, maintenance, EHS, contractors, and vendors.
  • Prepare schedule forecasts, look-ahead plans, dashboards, progress reports, milestone summaries, and executive 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, schedule risk assessments, earned-value analysis, or resource-loaded schedules is valuable.

Nice to have

  • Experience scheduling pharmaceutical manufacturing, laboratory, utility, packaging, warehouse, or facility-infrastructure projects.
  • Experience with brownfield projects in active GMP manufacturing environments.
  • Experience supporting shutdowns, equipment installations, technology transfers, or operational-readiness programs.
  • Knowledge of system turnover, commissioning plans, qualification protocols, and validation master plans.

Culture & Benefits

  • Employee-owned company with an inclusive culture focused on mutual respect and belonging.
  • International project delivery environment with opportunities to work across multidisciplinary teams.
  • Commitment to sustainability, corporate responsibility, inclusion, diversity, and accessible hiring.
  • Permanent or contract engagement options are available.

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