Вакансия из Hirify RU Global, списка компаний с восточно-европейскими корнями Для мэтча и отклика нужен Plus
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$130к-170к/год
$110к$150кмедиана$180к
По похожим ролям (49) ~ $150к/год
На СНГ рынке: $1.4к/мес ($735 - $1.8к)
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Роль четко описана в специализированной команде биотехнологической цепочки поставок и охватывает клинические исследования и коммерческие операции; привлекательность добавляют перспективная сфера и перечисленные льготы.
?Два направления
Понятные задачи
Биотехнологии
Расширенные льготы
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Manager, Supply Chain (Biotech): Managing end-to-end clinical trial and commercial supply chain operations with an accent on drug product delivery, packaging, regulatory coordination, and inventory continuity. Focus on critical-path planning, supplier collaboration, risk mitigation, and maintaining uninterrupted supply for clinical sites and commercial markets.
Location: Remote in the East Coast, US or in the UK. Applicants must have employment rights in the country to which they apply; employment visa sponsorship is not available.
Base salary: $130,000–$170,000 USD per annum, plus discretionary bonus and equity for permanent hires.
Company
hirify.global is a biotechnology company developing COMP360 synthetic psilocybin for treatment-resistant depression and post-traumatic stress disorder.
What you will do
Manage end-to-end manufacturing and supply chain operations for clinical trial and commercial materials.
Oversee bulk drug product delivery to distribution partners, including packaging, labelling, release, and shipping timelines.
Coordinate with clinical and commercial regulatory partners and distribution vendors to secure approvals and meet shipping deadlines.
Manage drug product shelf life and resupply to maintain continuity of supply for clinical study sites.
Set up and manage collaborations with worldwide clinical and commercial supply chain vendors while maintaining relationships with manufacturing and packaging partners.
Lead project planning, resource and budget management, risk mitigation, controls, monitoring, and reporting.
Requirements
Bachelor’s degree or equivalent in science, operations management, a closely related subject, or relevant industry experience.
Proven stakeholder management and excellent interpersonal and communication skills.
Working knowledge of GMP, GCP, and GDP.
Experience with project planning and risk management.
Understanding of clinical trial procedures and commercial supply chain operations.
Ability to respond to changing priorities and manage multiple tasks.
Permanent employment with flexible working arrangements and generous time off.
Parental and reproductive support, health and medical coverage, mental health and wellbeing support, and financial health benefits.
Inclusive equal-opportunity workplace with reasonable accommodation available during the interview process.
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