Назад
Company hidden
8 дней назад

Site Project Lead

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Singapore
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Site Project Lead (Pharmaceutical Manufacturing): Leading technology transfer and new production introduction projects at a Singapore manufacturing site with an accent on operational readiness, project governance, financial control, and regulatory compliance. Focus on planning and executing complex projects, coordinating cross-functional and global stakeholders, and delivering process startup objectives across cost, quality, HSE, and industrial performance.

Location: City of Singapore

Company

hirify.global develops medicines and applies science to improve health outcomes through pharmaceutical research and manufacturing.

What you will do

  • Lead technology transfer and new production introduction projects at the manufacturing site, acting as the NPI lead and project manager.
  • Define project objectives, scope, strategy, timelines, costs, and risks with project partners.
  • Coordinate end-to-end execution, project controls, deliverables, expenditures, changes, and risk management.
  • Drive site operational readiness for process startup and oversee performance across quality, HSE, deadlines, costs, and industrial objectives.
  • Manage communications with site, global, and external stakeholders and present project status to governance committees.
  • Maintain project progress and financial records in project management tools, including Shine, in line with auditable group 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 regulations and constraints, including GxP and FDA requirements.
  • At least 3 years of experience managing complex projects with significant budgets or team sizes in a manufacturing site environment.
  • At least 5 years of leadership experience with a record of building and leading cross-functional teams.
  • Experience with digital tools supporting project execution and monitoring, plus strong financial acumen and understanding of industrial strategy.

Culture & Benefits

  • Work in a supportive, future-focused environment centered on scientific progress.
  • Access opportunities for career growth through promotions or international and lateral moves.
  • Collaborate in a dynamic environment focused on continuous learning and professional development.
  • Contribute to process improvement and innovation with cross-functional partners.
  • Equal opportunity employment is provided regardless of protected personal characteristics.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →