Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль четко описана и предполагает полную ответственность за крупные проекты в фармацевтическом производстве и трансфер технологий; также указаны возможности развития и сильный пакет льгот в международной компании.
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Полный цикл
Развитие карьеры
Влияние на производство
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Описание вакансии
Текст:
Hirify AI/Оригинал
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.
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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