Sr Dir PMO Vision R&D

Role Summary

Senior Director, Vision R&D PMO responsible for leading the end-to-end execution of complex, cross-functional programs within the Vision R&D organization, with a focus on the Surgical Vision portfolio and building overall Project Management capabilities. This role ensures alignment with strategic goals, regulatory standards, and quality expectations. You will report directly to the Global Head of R&D, J&J Vision. Location options include Jacksonville, FL (Preferred); Irvine, CA; Milpitas, CA.

Responsibilities

• Lead a global New Product Development (NPD) PMO organization focused on Portfolio Management and Program Execution across the J&J Vision new product pipeline.
• Work closely with R&D, Global Strategic Marketing and functional leadership to create NPD portfolio strategies and an achievable execution plan.
• Lead NPD PMO programs from early-stage innovation concepts to product launch and ensure sustaining stability program metrics are achieved post-launch.
• Ensure delivery for NPD programs are on time, within scope, and on budget per plan.
• Lead and evolve the PMO function in R&D, growing project management skills and capabilities, establishing best practices & governance frameworks, and creating standardized tools to support consistent project execution.
• Act as a strategic partner to Technical Leads, Functional Managers, and Business Leaders to identify and mitigate technical and project risks.
• Ensure effective cross-functional collaboration across Global R&D sites and functional groups.
• Provide clear, timely communication of project status, risks, and mitigation plans to senior leadership and stakeholders.
• Ensure adequate resourcing and budget allocation across project portfolios.
• Inspire and lead a team of project managers, fostering a culture of excellence, compliance, and innovation.
• Champion a patient- and customer-centric mindset in all project execution activities.

Qualifications

• Required:
  • Bachelor’s degree in life sciences, engineering, or related field.
  • 10+ years of progressive experience in project / program management within a medical device environment.
  • Proven success in leading complex, cross-functional product development programs.
  • Understanding of regulatory requirements, quality standards, and product development lifecycles.
  • Strong leadership and stakeholder management skills, with the ability to influence across all levels of the organization.
  • Experience managing global teams is required.
• Preferred:
  • Advanced degree (MBA, MS, PhD) preferred.
  • PMP, Six Sigma or equivalent certification is highly preferred.
  • Process Excellence Certifications in Design for Six Sigma, DMADV, DMAIIC preferred.