Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Чётко описанная senior-позиция в продуктовой компании в сфере медицинского ИИ даёт значимую ответственность за программы и поддержку обучения, но работа только в офисе в Сеуле и отсутствие данных о зарплате оставляют важные условия неопределёнными.
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Зарплата не указанаТолько офисПонятные задачиМедицинский ИИПоддержка обучения
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Program Manager (AI/Medical Devices): Leading end-to-end programs for regulated medical AI products from development and validation through regulatory readiness, launch, and phase-out with an accent on cross-functional planning, governance, risk management, and stakeholder alignment. Focus on integrating interdependent workstreams, balancing technical, quality, regulatory, and business requirements, and supporting senior-level decision-making.
Location: On-site at hirify.global HQ, Gangnam-gu, Seoul, South Korea
Company
hirify.global is a medical AI software company developing AI-powered solutions for cancer detection and treatment outcome prediction.
What you will do
Translate company strategy and product objectives into program objectives, milestones, and integrated execution plans.
Lead end-to-end programs across product development, validation, regulatory readiness, launch, and phase-out.
Integrate multiple projects and workstreams while managing dependencies, risks, issues, timelines, scope, resources, quality, and regulatory requirements.
Align priorities and trade-offs across Product Management, AI Research, Engineering, Data, Clinical, Regulatory Affairs, Quality Assurance, Commercial, and other functions.
Establish program governance and provide senior leaders with visibility into status, risks, dependencies, and key decisions.
Improve program management processes and strengthen organizational execution capabilities.
Requirements
10+ years of relevant professional experience, including leadership of complex cross-functional programs.
Experience managing regulated products through development and commercialization.
Experience integrating interdependent projects and workstreams to achieve program-level outcomes.
Strong understanding of product lifecycle management, scope, schedule, risk, dependencies, and stakeholder coordination.
Experience balancing regulatory, quality, technical, and business requirements.
Professional proficiency in English; English resume and cover letter required.
Nice to have
Experience with medical device development, regulatory approval, and commercialization.
Experience with Software as a Medical Device, AI/ML-enabled medical devices, or digital health products.
Knowledge of Design Controls, Verification & Validation, Quality Management Systems, and regulatory processes.
Experience with global cross-functional programs or PMO/portfolio management.
Culture & Benefits
Full-time employment with a 3-month probation period.
Meal allowance of up to 12,000 KRW per meal when working at the office.
Latest computer equipment, including Macs and 4K monitors, renewable every three years.
Seminar registration fees, books, AI and medical seminars, and AI learning resources are supported.
In-house English lessons and up to 1.2 million KRW in annual benefits points.
Medical checkups, employee accident insurance, paid time off, and holiday and family-event allowances.
Hiring process
Document screening, online introductory interview, and online competency-based interview.
On-site panel interview followed by an on-site culture-fit interview.
Reference checks may be conducted after the final interview, followed by onboarding.
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