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Sr Dir PMO Vision R&D

Johnson & Johnson
On-site
Irvine, CA
$253,300 - $394,450 USD yearly
Operations

Role Summary

Senior Director, Vision R&D PMO leads end-to-end execution of complex cross-functional programs within the Vision R&D organization, focusing on the Surgical Vision portfolio and building overall Project Management capabilities. Location preferences include Jacksonville, FL (preferred); Irvine, CA and Milpitas, CA are also options.

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 concepts to product launch; ensure sustaining stability program metrics are achieved post-launch.
  • Ensure delivery for NPD programs is on time, within scope, and on budget per plan.
  • Lead and evolve the PMO function in R&D, growing project management skills, 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.
  • Required: 10+ years of progressive experience in project / program management within a medical device environment.
  • Required: Proven success in leading complex, cross-functional product development programs.
  • Required: Understanding of regulatory requirements, quality standards, and product development lifecycles.
  • Required: Strong leadership and stakeholder management skills, with the ability to influence across all levels of the organization.
  • Required: Experience managing global teams.

Preferred Qualifications

  • Advanced degree (MBA, MS, PhD) preferred.
  • PMP, Six Sigma or equivalent certification is highly preferred.
  • Process Excellence Certifications in Design for Six Sigma, DMADV, DMAIC preferred.

Education

  • Bachelor’s degree in life sciences, engineering, or related field.
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