1 день назад
Program Manager, R&D (MedTech)
118 000 - 203 550$
Мэтч & Сопровод
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Описание вакансии
Текст:
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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