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8 дней назад

Senior Program Manager (AI/Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
SK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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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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