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1 день назад

Program Manager, R&D (MedTech)

118 000 - 203 550$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Program Manager, R&D (MedTech): Leading the Monarch Bronchoscopy product development program with an accent on cross-functional execution, integrated planning, and risk mitigation. Focus on driving milestones within budget and timelines, coordinating engineering and external vendor teams, and communicating progress to management.

Location: Santa Clara, California, United States of America; this position must be located in Santa Clara, CA. Hybrid work is indicated.

Salary: $118,000–$203,550 per year

Company

Johnson & Johnson MedTech develops innovative surgical technologies and personalized, less invasive healthcare solutions, including robotics and digital surgery products.

What you will do

  • Own and drive the Monarch Bronchoscopy product development program.
  • Develop and manage integrated project timelines, budgets, quarterly goals, milestones, and action items.
  • Lead cross-functional meetings and teams, resolve or escalate issues, and build ownership of project objectives.
  • Identify technical and program risks, create mitigation plans, and facilitate risk closure.
  • Communicate project progress to directors, managers, and the J&J Robotics & Digital Solutions management team.
  • Coordinate external vendors, including co-development and subcontracted development activities.

Requirements

  • BS or BA in Engineering or a related technical field.
  • 7+ years of experience in a regulated environment and 3+ years in program or project management.
  • Experience working with complex systems or complex, dynamic teams.
  • Experience using or administering project management software.
  • Strong written and verbal communication skills, self-motivation, urgency, and ability to present to different audiences and organizational levels.
  • Ability to travel up to 10% domestically and internationally.

Nice to have

  • MS or PhD in Engineering, Science, or Business.
  • Experience leading early-stage development teams and contributing to business cases or user requirements.
  • Experience with Medical Device Design Control, QSR 21 CFR Part 820, FDA and 510(k) regulatory strategies, or CE Mark.
  • Engineering experience in medical device design and development.
  • PMP certification.

Culture & Benefits

  • Inclusive work environment focused on healthcare innovation and patient outcomes.
  • Participation in a consolidated retirement plan, pension, and 401(k) savings plan.
  • Eligibility for the long-term incentive program.
  • Vacation, sick time, holidays, personal and family time, parental, bereavement, caregiver, volunteer, and military spouse leave.

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