Hybrid Project Lead, MedTech Innovations & Partnerships

Johnson & Johnson Co.; Raritan (NJ); Hybrid; USD 102,000 - 177,000; Full time

Benefits offered by this job

Pension plan

401(k) plan

Generous paid time off

Job summary

Johnson & Johnson MedTech is recruiting for a Project Lead, Innovation & Partnerships in Medtech. The role can be based in Cincinnati, OH or Raritan, NJ and will operate on a Flex/Hybrid schedule with 3 days on-site.

You will lead external collaborations, drive program execution, and align regulatory, quality, and manufacturing activities to bring complex medical devices from concept to market.

Qualifications

• Bachelor’s degree in engineering is required; advanced degree preferred.
• 7+ years in medical device development, with experience in combination products or related fields is required.
• Proven record of delivering technically complex products from concept to market.
• PM proficiency with PMP or similar certification and project management tools is required.
• Willingness to travel approximately 10%.

Responsibilities

• Lead cross-functional JJMT teams on parallel product development projects with JJIM.
• Meet performance agreement requirements: time to market, cost of goods, development costs, quality and market size forecast.
• Lead external and inter-company collaboration projects from assessment to lifecycle transfer.
• Drive technical direction within cross-functional teams, balancing rigor with business needs.
• Identify risks early and implement mitigation strategies in a regulated environment.

Skills

Project leadership

Cross-functional collaboration

Regulatory knowledge

Data-driven decisions

Risk management

Vendor collaboration

Education

Bachelor's degree in engineering

Master’s or Ph.D. in biomedical/mechanical/electrical engineering

Tools

PMP

Smartsheet

MS Project

Job description

Johnson & Johnson MedTech is recruiting for a Project Lead, Innovation & Partnerships in Medtech. The role can be based in Cincinnati, OH or Raritan, NJ and will operate on a Flex/Hybrid schedule with 3 days on-site.

You will lead external collaborations, drive program execution, and align regulatory, quality, and manufacturing activities to bring complex medical devices from concept to market.