Назад
Company hidden
6 дней назад

Project Head, Energy and Endo-mechanical Platforms, R&D - MedTech

137 000 - 235 750$
Формат работы
hybrid
Тип работы
fulltime
Грейд
head
Английский
b2
Страна
US
Релокация
US
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
Project Head, Energy and Endo-mechanical Platforms, R&D - MedTech (Medical Devices): Leading end-to-end delivery of regulated new product development programs for surgical technologies with an accent on cross-functional execution, regulatory requirements, and program risk management. Focus on driving scope, schedule, and cost decisions, resolving complex organizational challenges, and bringing Class II and Class III medical devices through market introduction.

Location: Cincinnati, Ohio, United States; Flex/Hybrid schedule with 3 days per week on-site. Up to 20% domestic and international travel required. Relocation assistance may be provided for highly qualified individuals.

Salary: $137,000–$235,750 per year

Company

Johnson & Johnson MedTech develops surgical technologies and solutions, including surgical staplers, clip appliers, trocars, and sealing devices for minimally invasive and open surgical procedures.

What you will do

  • Lead end-to-end execution and delivery of new product development programs, managing scope, schedule, cost, and resources.
  • Plan, track, and communicate program status while identifying risks, creating mitigation plans, and accelerating progress.
  • Coordinate cross-functional execution across R&D, Supply Chain, Quality, Regulatory, Clinical, Finance, and Marketing.
  • Establish operating rhythms, core team meetings, milestone planning, and clear accountability.
  • Develop scenarios, assess trade-offs, secure decisions, escalate risks, and resolve cross-functional challenges.
  • Build an inclusive, high-performing team culture focused on shared ownership and sustained performance.

Requirements

  • Bachelor’s degree in an engineering or scientific discipline; an advanced degree is preferred.
  • At least 10 years of new product development experience and at least 3 years in a regulated industry.
  • Demonstrated success leading regulated programs through market introduction.
  • Experience leading and influencing across complex, matrixed organizations, with strong strategic planning and operational execution skills.
  • Understanding of medical device development and global regulatory and clinical requirements.
  • Ability to work in Cincinnati with three days per week on-site and travel domestically and internationally up to 20%.

Nice to have

  • Experience with Class II and/or Class III medical devices.
  • Previous R&D team leadership, including direct or indirect people leadership.
  • Experience leading through change, navigating ambiguity, developing talent, and building inclusive team cultures.
  • Advanced degree in an engineering or scientific discipline.

Culture & Benefits

  • Inclusive work environment focused on diversity, dignity, psychological safety, and shared ownership.
  • Participation in pension and 401(k) savings plans, subject to plan terms.
  • Vacation, sick time, holidays, personal and family time, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time-off.

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 →