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7 дней назад

Site Project Lead (Pharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
China
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
Site Project Lead (Pharmaceutical Manufacturing): Leading end-to-end site projects and technology transfers for new pharmaceutical products and processes in Hangzhou with an accent on project planning, process assessment, scale-up, validation, GMP compliance, and cross-functional coordination. Focus on managing complex manufacturing projects, aligning local capabilities with transferred processes, controlling budgets and risks, and supporting regulatory submissions.

Location: Hangzhou, China

Company

hirify.global is a global healthcare company focused on applying science to improve patients’ lives.

What you will do

  • Develop project objectives, scope, strategy, timelines, costs, deliverables, and risk plans with partners.
  • Lead and monitor end-to-end execution of one or more site projects, including project controls, reporting, change management, and governance reviews.
  • Manage site and global stakeholders and coordinate with operational, support, external, and related project contacts.
  • Lead technology transfer planning, timeline tracking, risk management, process and technical assessments, and gap analyses for products and processes transferred to the local manufacturing site.
  • Organize and support scale-up, trial runs, engineering batches, registration batches, and process validation batches.
  • Support regulatory submissions and ensure technology transfers comply with GMP and quality-system requirements.

Requirements

  • Scientific bachelor’s degree, preferably in chemical, biochemical, or pharmaceutical engineering, or a degree in business or finance.
  • At least 5 years of total industry experience with exposure to production, supply chain, chemical engineering, process technology, project investment, finance, quality, and regulatory requirements.
  • Good knowledge of pharmaceutical-industry constraints and regulations, including GxP and FDA requirements.
  • Strong project management and project portfolio management knowledge in a manufacturing-site environment, with 3+ years of experience managing complex projects with significant budgets and/or significant team size.
  • At least 5 years of leadership experience with a proven record of building and leading cross-functional teams.
  • Experience with and agility in using digital tools for project execution and monitoring.
  • Financial acumen and understanding of industrial strategy to develop project strategies and business cases.

Culture & Benefits

  • Values include aiming higher, acting for patients, being bold, and leading together.
  • Supportive, future-focused environment with opportunities for promotion, lateral moves, and international career development.
  • Rewards package recognizing individual contribution.
  • Health and wellbeing benefits, including healthcare, prevention and wellness programs, and at least 14 weeks of gender-neutral parental leave.
  • Equal-opportunity employer committed to inclusion regardless of protected characteristics.

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