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Senior Engineering Project Manager (Pharmaceutical Engineering)

52 000
Формат работы
remote (только Italy)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
France/Italy/Brazil
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
Senior Engineering Project Manager (Pharmaceutical Engineering): Leading medium and large-scale capital and process engineering projects in pharmaceutical manufacturing with an accent on GMP compliance, validation, regulatory alignment, and operational excellence. Focus on coordinating cross-functional teams, managing design through qualification and handover, controlling budgets and risks, and delivering facility expansions, cleanroom construction, and equipment upgrades.

Location: Parma, Italy

Salary: €52,000 minimum annual salary, plus annual performance bonus and benefits.

Company

hirify.global is an international research-focused biopharmaceutical group operating in more than 30 countries, with manufacturing and supply operations across pharmaceutical production sites.

What you will do

  • Lead medium and large-scale capital and process engineering projects, including facility expansions, cleanroom construction, equipment upgrades, and process implementation.
  • Define project scope, timelines, budgets, and resource allocation strategies.
  • Coordinate Engineering, Quality Assurance, Validation, Manufacturing, HSE, and Regulatory Affairs teams.
  • Oversee design, procurement, construction, commissioning, qualification, and handover activities.
  • Manage contractors, EPC partners, equipment vendors, project risks, milestones, KPIs, and financial performance.
  • Lead governance meetings, report to senior leadership, and drive continuous improvement in project delivery.

Requirements

  • Bachelor’s degree in Chemical, Mechanical, Industrial, or related Engineering.
  • 10–12+ years of engineering or project management experience in the pharmaceutical or life sciences industry.
  • Strong knowledge of GMP, validation processes, and FDA or EMA regulatory frameworks.
  • Experience managing capital projects in regulated environments.
  • Leadership experience with cross-functional and international teams.
  • Strong communication and stakeholder management skills.

Nice to have

  • Master’s degree or MBA.
  • PMP or PRINCE2 certification.
  • Experience with biologics, sterile manufacturing, API production, MES, SAP, sustainability, or energy optimization projects.

Culture & Benefits

  • Benefits include pension, private medical insurance, wellbeing programmes, flexible benefits, and ticket restaurant support.
  • Flexible working arrangements and remote work options are available.
  • Relocation support and tax assistance services are offered for foreign colleagues.
  • Access to training and professional development resources.
  • Work-life balance initiatives and performance-based bonuses.

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