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4 дня назад

TPM Project Manager (Technical Transfer)

Формат работы
hybrid
Тип работы
fulltime
Английский
b2
Страна
UK
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
TPM Project Manager (Technical Transfer): Leading cross-functional Technical Operations projects from initiation through closure in a regulated pharmaceutical environment with an accent on integrated planning, governance, risk control, and stakeholder alignment. Focus on coordinating technical, quality, and regulatory dependencies, interpreting delivery data, and driving compliant, sustainable project outcomes.

Location: UK; must be flexible to commute to the Cambridge office for important meetings and updates

Company

hirify.global is a global healthcare company developing and delivering innovative treatments in pain management, infectious disease, and other severe and debilitating disease areas.

What you will do

  • Own end-to-end delivery of assigned Technical Transfer and Technical Operations projects from initiation through closure.
  • Define scope, milestones, workstreams, resources, dependencies, budgets, and success measures; maintain integrated delivery plans.
  • Establish project governance and manage risks, issues, assumptions, dependencies, changes, decisions, and actions.
  • Lead cross-functional stakeholders, facilitate project meetings and decision forums, and resolve delivery barriers.
  • Track schedule, resources, budget, quality, benefits, and delivery health; provide evidence-based reporting and recovery options.
  • Embed change management, adoption, compliance, lessons learned, and continuous improvement into project delivery.

Requirements

  • Bachelor's degree or equivalent relevant professional experience in project management, engineering, science, operations, supply chain, business, or a related discipline.
  • Demonstrable experience delivering complex Technical Transfer projects or cross-functional projects in Technical Operations, manufacturing, supply chain, engineering, quality, pharmaceuticals, or a similar regulated environment.
  • Experience managing projects requiring working knowledge of Technical, Quality, and Regulatory aspects.
  • Experience managing integrated plans, governance, risks, budgets, and senior stakeholders.
  • Strong project leadership, planning, facilitation, problem-solving, communication, and influencing skills without direct authority.
  • Ability to interpret data, identify trends, and translate complexity into clear decisions and actions.
  • Sound commercial and financial awareness.
  • Proficiency with standard project-planning, reporting, and collaboration tools.
  • Working knowledge of regulated quality and compliance expectations, with a focus on patients, integrity, and delivery.

Nice to have

  • Transformation experience.

Culture & Benefits

  • 12-month contingent contract through PAYE or Umbrella on a daily-rate basis.
  • Collaborative and inclusive work environment focused on integrity, patient-centricity, dignity, and respect.
  • Learning and development opportunities through a varied programme.

Hiring process

  • Applications are considered for the 12-month contingent contract; an independent consultant arrangement is specified.

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